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dbVar

Database of genomic structural variation

nsv5614279

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

Submitted genomic65,238,655-65,238,655

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5614279	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	65,238,655	65,238,655
nsv5614279	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	65,465,789	65,465,789

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17113548	insertion	SAMN01096687	Sequencing	Sequence alignment	1,334

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17113548	Submitted genomic		NC_000002.12:g.652 38655_65238656ins3 216	GRCh38 (hg38)		NC_000002.12	Chr2	65,238,655	65,238,655
nssv17113548	Remapped	Perfect	NC_000002.11:g.654 65789_65465790ins3 216	GRCh37.p13	First Pass	NC_000002.11	Chr2	65,465,789	65,465,789

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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