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dbVar

Database of genomic structural variation

nsv5984023

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:67

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: 91 SVs from 21 studies. See in: genome view

Submitted genomic32,326,235-32,326,301

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5984023	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	32,326,235	32,326,301
nsv5984023	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	32,791,836	32,791,902

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17528693	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17528693	Submitted genomic		NC_000001.11:g.323 26235_32326301del	GRCh38 (hg38)		NC_000001.11	Chr1	32,326,235	32,326,301
nssv17528693	Remapped	Perfect	NC_000001.10:g.327 91836_32791902del	GRCh37.p13	First Pass	NC_000001.10	Chr1	32,791,836	32,791,902

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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