A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568926



Internal ID16009649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34376256..34403609hg38UCSC Ensembl
Innerchr15:34668457..34695810hg19UCSC Ensembl
Innerchr15:32455749..32483102hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3827354
hg1927354
hg1827354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839802
Samples
Known GenesGOLGA8A, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568926
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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