A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149271



Internal ID15875229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101387672..101591019hg38UCSC Ensembl
Innerchr15:101927877..102131222hg19UCSC Ensembl
Innerchr15:99745400..99948745hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38203348
hg19203346
hg18203346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570850
Supporting Variants
SamplesHGDP00654
Known GenesPCSK6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149271
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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