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dbVar

Database of genomic structural variation

nsv5650629

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: 101 SVs from 18 studies. See in: genome view

Submitted genomic40,024,228-40,024,228

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5650629	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	40,024,228	40,024,228
nsv5650629	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	40,316,429	40,316,429

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17095989	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17095989	Submitted genomic		NC_000015.10:g.400 24228_40024229ins3 23	GRCh38 (hg38)		NC_000015.10	Chr15	40,024,228	40,024,228
nssv17095989	Remapped	Perfect	NC_000015.9:g.4031 6429_40316430ins32 3	GRCh37.p13	First Pass	NC_000015.9	Chr15	40,316,429	40,316,429

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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