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dbVar

Database of genomic structural variation

nsv6086819

Organism: Homo sapiens

Study:nstd212 (Wu 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):Wu 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: 125 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
nsv6086819	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	100,873,455	100,873,455
nsv6086819	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	Method	Analysis
nssv17610741	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17610741	Submitted genomic		NC_000014.9:g.1008 73455_100873456ins 1144	GRCh38 (hg38)		NC_000014.9	Chr14	100,873,455	100,873,455
nssv17610741	Remapped	Perfect	NC_000014.8:g.1013 39792_101339793ins 1144	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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