A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570284



Internal ID16357693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84037445..84164180hg38UCSC Ensembl
Innerchr15:84706197..84832932hg19UCSC Ensembl
Innerchr15:82497201..82623936hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38126736
hg19126736
hg18126736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149250
SamplesHGDP00208
Known GenesADAMTSL3, EFTUD1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570284
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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