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dbVar

Database of genomic structural variation

nsv5659293

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: 133 SVs from 42 studies. See in: genome view

Submitted genomic67,989,353-67,989,353

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659293	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	67,989,353	67,989,353
nsv5659293	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	67,756,824	67,756,824

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17075470	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
nssv17075470	Submitted genomic		NC_000011.10:g.679 89353_67989354ins5 3	GRCh38 (hg38)		NC_000011.10	Chr11	67,989,353	67,989,353
nssv17075470	Remapped	Perfect	NC_000011.9:g.6775 6824_67756825ins53	GRCh37.p13	First Pass	NC_000011.9	Chr11	67,756,824	67,756,824

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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