A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568662



Internal ID16009385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27726493..29056123hg38UCSC Ensembl
Innerchr15:27971639..29348326hg19UCSC Ensembl
Innerchr15:25645234..27135618hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381329631
hg191376688
hg181490385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839289
Samples
Known GenesAPBA2, GOLGA6L7P, GOLGA8F, GOLGA8G, GOLGA8M, HERC2, HERC2P9, LOC100289656, LOC646278, MIR4509-1, MIR4509-2, MIR4509-3, OCA2, WHAMMP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568662
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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