A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695113



Internal ID15085079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132431339..132441869hg38UCSC Ensembl
Innerchr3:132150183..132160713hg19UCSC Ensembl
Innerchr3:133632873..133643403hg18UCSC Ensembl
Innerchr3:133632881..133643411hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3810531
hg1910531
hg1810531
hg1710531
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522333
Supporting Variants
Samples
Known GenesDNAJC13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695113
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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