A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660731



Internal ID15050697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55592737..55674892hg38UCSC Ensembl
Innerchr11:55360213..55442368hg19UCSC Ensembl
Innerchr11:55116789..55198944hg18UCSC Ensembl
Innerchr11:55116789..55198944hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3882156
hg1982156
hg1882156
hg1782156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660731
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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