A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568925



Internal ID16009648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34374874..34379904hg38UCSC Ensembl
Innerchr15:34667075..34672105hg19UCSC Ensembl
Innerchr15:32454367..32459397hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385031
hg195031
hg185031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839801
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568925
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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