A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149124



Internal ID15533694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34579095hg38UCSC Ensembl
Innerchr15:34718594..34871296hg19UCSC Ensembl
Innerchr15:32505886..32658588hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38152703
hg19152703
hg18152703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569004
Supporting Variants
SamplesNINDS_202
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149124
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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