A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972950



Internal ID18261480
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758638, nssv2757806, nssv2760037, nssv2762252, nssv2759222, nssv2766459
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP00998, HGDP01307, HGDP00665
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972950
Frequency
Sample Size10
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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