A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2760037



Internal ID17483406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55590444..55712348hg38UCSC Ensembl
Innerchr11:55357920..55479824hg19UCSC Ensembl
Innerchr11:55114496..55236400hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38121905
hg19121905
hg18121905
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972950
Supporting Variants
SamplesHGDP00998
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2760037
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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