A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570110



Internal ID16357519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76679115..76828855hg38UCSC Ensembl
Innerchr15:76971456..77121196hg19UCSC Ensembl
Innerchr15:74758511..74908251hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38149741
hg19149741
hg18149741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149155
SamplesHGDP00183
Known GenesSCAPER
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570110
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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