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dbVar

Database of genomic structural variation

nsv5989582

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:134,158

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: 585 SVs from 68 studies. See in: genome view

Submitted genomic56,964,251-57,098,408

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5989582	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	56,964,251	57,098,408
nsv5989582	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	57,191,386	57,325,543

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17532529	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17532529	Submitted genomic		NC_000002.12:g.569 64251_57098408del	GRCh38 (hg38)		NC_000002.12	Chr2	56,964,251	57,098,408
nssv17532529	Remapped	Perfect	NC_000002.11:g.571 91386_57325543del	GRCh37.p13	First Pass	NC_000002.11	Chr2	57,191,386	57,325,543

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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