A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518289



Internal ID15098896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84164180..84570741hg38UCSC Ensembl
Innerchr15:84832932..85113972hg19UCSC Ensembl
Innerchr15:82623936..82914976hg18UCSC Ensembl
Innerchr15:82623936..82914976hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38406562
hg19281041
hg18291041
hg17291041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695720
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LINC00933, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518289
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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