A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566959



Internal ID21759002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46316384..46322790hg38UCSC Ensembl
chr7:46355982..46362388hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg386407
hg196407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566959
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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