A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518707



Internal ID15099314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43509826..43534359hg38UCSC Ensembl
Innerchr15:43802024..43826557hg19UCSC Ensembl
Innerchr15:41589316..41613849hg18UCSC Ensembl
Innerchr15:41589316..41613849hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3824534
hg1924534
hg1824534
hg1724534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696158
Samples
Known GenesMAP1A, PPIP5K1, RNU6-28P, TP53BP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518707
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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