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dbVar

Database of genomic structural variation

nsv5660874

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 141 SVs from 31 studies. See in: genome view

Submitted genomic35,350,843-35,350,843

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5660874	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	35,350,843	35,350,843
nsv5660874	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	35,841,746	35,841,746

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17104298	insertion	SAMN00004622	Sequencing	Sequence alignment	1,208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17104298	Submitted genomic		NC_000019.10:g.353 50843_35350844ins8 13	GRCh38 (hg38)		NC_000019.10	Chr19	35,350,843	35,350,843
nssv17104298	Remapped	Perfect	NC_000019.9:g.3584 1746_35841747ins81 3	GRCh37.p13	First Pass	NC_000019.9	Chr19	35,841,746	35,841,746

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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