A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696163



Internal ID15086129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52497607..52520266hg38UCSC Ensembl
Innerchr6:52362405..52385064hg19UCSC Ensembl
Innerchr6:52470364..52493023hg18UCSC Ensembl
Innerchr6:52470364..52493023hg17UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3822660
hg1922660
hg1822660
hg1722660
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518713
Supporting Variants
Samples
Known GenesTRAM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696163
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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