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dbVar

Database of genomic structural variation

nsv5546914

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Byrska-Bishop et al. 2022

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 298 SVs from 54 studies. See in: genome view

Submitted genomic15,674,441-15,674,441

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5546914	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	15,674,441	15,674,441
nsv5546914	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	15,785,251	15,785,251

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17721791	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17721791	Submitted genomic		NC_000019.10:g.156 74441_15674442ins2 20	GRCh38 (hg38)		NC_000019.10	Chr19	15,674,441	15,674,441
nssv17721791	Remapped	Perfect	NC_000019.9:g.1578 5251_15785252ins22 0	GRCh37.p13	First Pass	NC_000019.9	Chr19	15,785,251	15,785,251

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17721791	0.95	5572	5864

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