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dbVar

Database of genomic structural variation

nsv5655061

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: 210 SVs from 38 studies. See in: genome view

Submitted genomic44,975,659-44,975,659

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5655061	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	44,975,659	44,975,659
nsv5655061	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	45,267,857	45,267,857

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17097304	insertion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17097304	Submitted genomic		NC_000015.10:g.449 75659_44975660ins3 22	GRCh38 (hg38)		NC_000015.10	Chr15	44,975,659	44,975,659
nssv17097304	Remapped	Perfect	NC_000015.9:g.4526 7857_45267858ins32 2	GRCh37.p13	First Pass	NC_000015.9	Chr15	45,267,857	45,267,857

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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