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dbVar

Database of genomic structural variation

nsv5649609

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: 177 SVs from 34 studies. See in: genome view

Submitted genomic69,820,424-69,820,424

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5649609	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	69,820,424	69,820,424
nsv5649609	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	69,854,327	69,854,327

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17095339	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17095339	Submitted genomic		NC_000016.10:g.698 20424_69820425ins5 5	GRCh38 (hg38)		NC_000016.10	Chr16	69,820,424	69,820,424
nssv17095339	Remapped	Perfect	NC_000016.9:g.6985 4327_69854328ins55	GRCh37.p13	First Pass	NC_000016.9	Chr16	69,854,327	69,854,327

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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