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dbVar

Database of genomic structural variation

nsv6031606

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:134

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: 104 SVs from 27 studies. See in: genome view

Submitted genomic64,464,171-64,464,304

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6031606	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	64,464,171	64,464,304
nsv6031606	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	64,930,889	64,931,022

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17605296	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17605296	Submitted genomic		NC_000014.9:g.6446 4171_64464304del	GRCh38 (hg38)		NC_000014.9	Chr14	64,464,171	64,464,304
nssv17605296	Remapped	Perfect	NC_000014.8:g.6493 0889_64931022del	GRCh37.p13	First Pass	NC_000014.8	Chr14	64,930,889	64,931,022

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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