A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515522



Internal ID15443133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65279848..65304392hg38UCSC Ensembl
Innerchr14:65746566..65771110hg19UCSC Ensembl
Innerchr14:64816319..64840863hg18UCSC Ensembl
Innerchr14:64816319..64840863hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3824545
hg1924545
hg1824545
hg1724545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658440, nssv656028, nssv675842, nssv679920, nssv665307, nssv686866, nssv689550, nssv670586, nssv657532, nssv690494, nssv690864, nssv693981, nssv664365, nssv657808, nssv681754, nssv653450, nssv668449, nssv676196, nssv660195, nssv685398, nssv665039, nssv679167, nssv678644, nssv674384, nssv672156, nssv688480, nssv691692, nssv661048, nssv679494, nssv691645, nssv675071, nssv678881, nssv658852, nssv664892, nssv672028, nssv661252, nssv680286, nssv690255, nssv662653, nssv655627, nssv654386, nssv676484, nssv666296, nssv659113, nssv663319, nssv679353, nssv670449, nssv675725
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515522
Frequency
Sample Size2026
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


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