A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515774



Internal ID15442831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158547563..158551602hg38UCSC Ensembl
Innerchr1:158517353..158521392hg19UCSC Ensembl
Innerchr1:156783977..156788016hg18UCSC Ensembl
Innerchr1:155330426..155334465hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384040
hg194040
hg184040
hg174040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688038, nssv662523, nssv653320, nssv657768, nssv658359, nssv677418, nssv666508, nssv673661, nssv684385, nssv685281, nssv691244, nssv665816, nssv658814, nssv653201, nssv673173, nssv661057, nssv668164, nssv686215, nssv681388, nssv675221, nssv669489, nssv668037, nssv667134, nssv657961, nssv665854, nssv690472, nssv690060, nssv670410, nssv656382, nssv686592, nssv658243, nssv662802, nssv665984, nssv657291, nssv693812, nssv682898, nssv687858, nssv689056, nssv673767, nssv688513, nssv652086
Samples
Known GenesOR6Y1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515774
Frequency
Sample Size2026
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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