A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652955



Internal ID15042921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55592737..55702527hg38UCSC Ensembl
Innerchr11:55360213..55470003hg19UCSC Ensembl
Innerchr11:55116789..55226579hg18UCSC Ensembl
Innerchr11:55116789..55226579hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38109791
hg19109791
hg18109791
hg17109791
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)nssv652955
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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