A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851156



Internal ID15798426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101488742..101754031hg38UCSC Ensembl
Innerchr15:102028947..102294234hg19UCSC Ensembl
Innerchr15:99846470..100111757hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38265290
hg19265288
hg18265288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570869
Supporting Variants
Samples
Known GenesPCSK6, TARSL2, TM2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851156
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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