A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702556



Internal ID15092522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44988875..45020470hg38UCSC Ensembl
Innerchr21:46408790..46440385hg19UCSC Ensembl
Innerchr21:45233218..45264813hg18UCSC Ensembl
Innerchr21:45233218..45264813hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3831596
hg1931596
hg1831596
hg1731596
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526277
Supporting Variants
Samples
Known GenesLINC00162, LINC00163
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702556
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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