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dbVar

Database of genomic structural variation

nsv6088617

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: 108 SVs from 20 studies. See in: genome view

Submitted genomic50,252,489-50,252,489

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6088617	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	50,252,489	50,252,489
nsv6088617	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	50,286,400	50,286,400

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17632961	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17632961	Submitted genomic		NC_000016.10:g.502 52489_50252490ins6 9	GRCh38 (hg38)		NC_000016.10	Chr16	50,252,489	50,252,489
nssv17632961	Remapped	Perfect	NC_000016.9:g.5028 6400_50286401ins69	GRCh37.p13	First Pass	NC_000016.9	Chr16	50,286,400	50,286,400

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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