A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701777



Internal ID15438429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33546113..33619232hg38UCSC Ensembl
Innerchr3:33587605..33660724hg19UCSC Ensembl
Innerchr3:33562609..33635728hg18UCSC Ensembl
Innerchr3:33562609..33635728hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3873120
hg1973120
hg1873120
hg1773120
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525628
Supporting Variants
Samples
Known GenesCLASP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701777
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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