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dbVar

Database of genomic structural variation

nsv5657988

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: 85 SVs from 24 studies. See in: genome view

Submitted genomic75,727,030-75,727,030

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5657988	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	75,727,030	75,727,030
nsv5657988	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	75,438,075	75,438,075

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17075893	insertion	SAMN00001229	Sequencing	Sequence alignment	1,149

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17075893	Submitted genomic		NC_000011.10:g.757 27030_75727031ins1 59	GRCh38 (hg38)		NC_000011.10	Chr11	75,727,030	75,727,030
nssv17075893	Remapped	Perfect	NC_000011.9:g.7543 8075_75438076ins15 9	GRCh37.p13	First Pass	NC_000011.9	Chr11	75,438,075	75,438,075

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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