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dbVar

Database of genomic structural variation

nsv5975623

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 150 SVs from 33 studies. See in: genome view

Submitted genomic84,910,928-84,910,928

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5975623	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	84,910,928	84,910,928
nsv5975623	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	85,304,707	85,304,707

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17365549	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17365549	Submitted genomic		NC_000012.12:g.849 10928_84910929ins6 0	GRCh38 (hg38)		NC_000012.12	Chr12	84,910,928	84,910,928
nssv17365549	Remapped	Perfect	NC_000012.11:g.853 04707_85304708ins6 0	GRCh37.p13	First Pass	NC_000012.11	Chr12	85,304,707	85,304,707

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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