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dbVar

Database of genomic structural variation

nsv6071234

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: 120 SVs from 23 studies. See in: genome view

Submitted genomic142,928,591-142,928,591

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6071234	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	142,928,591	142,928,591
nsv6071234	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	142,647,433	142,647,433

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17542372	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17542372	Submitted genomic		NC_000003.12:g.142 928591_142928592in s308	GRCh38 (hg38)		NC_000003.12	Chr3	142,928,591	142,928,591
nssv17542372	Remapped	Perfect	NC_000003.11:g.142 647433_142647434in s308	GRCh37.p13	First Pass	NC_000003.11	Chr3	142,647,433	142,647,433

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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