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dbVar

Database of genomic structural variation

nsv5625984

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: 183 SVs from 22 studies. See in: genome view

Submitted genomic94,695,713-94,695,713

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5625984	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	94,695,713	94,695,713
nsv5625984	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	95,707,941	95,707,941

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17149143	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17149143	Submitted genomic		NC_000008.11:g.946 95713_94695714ins6 4	GRCh38 (hg38)		NC_000008.11	Chr8	94,695,713	94,695,713
nssv17149143	Remapped	Perfect	NC_000008.10:g.957 07941_95707942ins6 4	GRCh37.p13	First Pass	NC_000008.10	Chr8	95,707,941	95,707,941

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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