A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656038



Internal ID15392690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67734155..67981346hg38UCSC Ensembl
Innerchr11:67501626..67748817hg19UCSC Ensembl
Innerchr11:67258202..67505393hg18UCSC Ensembl
Innerchr11:67258202..67505393hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38247192
hg19247192
hg18247192
hg17247192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516191
Supporting Variants
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656038
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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