A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699186



Internal ID15435838
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523431
Supporting Variants
Samples
Known GenesABTB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699186
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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