A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570779



Internal ID16011502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100201823..100595854hg38UCSC Ensembl
Innerchr15:100742028..101136059hg19UCSC Ensembl
Innerchr15:98559551..98953582hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38394032
hg19394032
hg18394032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148886
SamplesHGDP00064
Known GenesADAMTS17, CERS3, LINS, PRKXP1, SPATA41
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570779
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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