A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515795



Internal ID15442852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113396099..113402203hg38UCSC Ensembl
Innerchr11:113266821..113272925hg19UCSC Ensembl
Innerchr11:112772031..112778135hg18UCSC Ensembl
Innerchr11:112772031..112778135hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg386105
hg196105
hg186105
hg176105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672236, nssv658707, nssv665163, nssv678843, nssv690263, nssv684686, nssv656198, nssv687925, nssv682317, nssv664816, nssv680956, nssv674969, nssv677211, nssv671512, nssv659262, nssv682394, nssv674627, nssv674741, nssv675081, nssv693486, nssv658966, nssv691216, nssv669920, nssv687146, nssv688020, nssv663812, nssv665487, nssv673389
Samples
Known GenesANKK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515795
Frequency
Sample Size2026
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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