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dbVar

Database of genomic structural variation

nsv6063854

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: 147 SVs from 45 studies. See in: genome view

Submitted genomic133,785,312-133,785,312

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6063854	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	133,785,312	133,785,312
nsv6063854	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	133,504,156	133,504,156

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17549815	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17549815	Submitted genomic		NC_000003.12:g.133 785312_133785313in s80	GRCh38 (hg38)		NC_000003.12	Chr3	133,785,312	133,785,312
nssv17549815	Remapped	Perfect	NC_000003.11:g.133 504156_133504157in s80	GRCh37.p13	First Pass	NC_000003.11	Chr3	133,504,156	133,504,156

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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