A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523431



Internal ID15450724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34170545..34178302hg38UCSC Ensembl
Innerchr11:34192092..34199849hg19UCSC Ensembl
Innerchr11:34148668..34156425hg18UCSC Ensembl
Innerchr11:34148668..34156425hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387758
hg197758
hg187758
hg177758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699186
Samples
Known GenesABTB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523431
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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