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dbVar

Database of genomic structural variation

nsv5650391

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: 126 SVs from 31 studies. See in: genome view

Submitted genomic100,873,455-100,873,455

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5650391	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	100,873,455	100,873,455
nsv5650391	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	101,339,792	101,339,792

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17083363	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17083363	Submitted genomic		NC_000014.9:g.1008 73455_100873456ins 1589	GRCh38 (hg38)		NC_000014.9	Chr14	100,873,455	100,873,455
nssv17083363	Remapped	Perfect	NC_000014.8:g.1013 39792_101339793ins 1589	GRCh37.p13	First Pass	NC_000014.8	Chr14	101,339,792	101,339,792

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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