A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531649



Internal ID21856005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206172917..206173038hg38UCSC Ensembl
chr2:207037641..207037762hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987860
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531649
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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