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dbVar

Database of genomic structural variation

nsv6064377

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: 111 SVs from 19 studies. See in: genome view

Submitted genomic142,932,702-142,932,702

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6064377	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	142,932,702	142,932,702
nsv6064377	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	142,651,544	142,651,544

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17555005	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17555005	Submitted genomic		NC_000003.12:g.142 932702_142932703in s292	GRCh38 (hg38)		NC_000003.12	Chr3	142,932,702	142,932,702
nssv17555005	Remapped	Perfect	NC_000003.11:g.142 651544_142651545in s292	GRCh37.p13	First Pass	NC_000003.11	Chr3	142,651,544	142,651,544

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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