A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv840369



Internal ID15787639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34450638..34690183hg38UCSC Ensembl
Innerchr15:34742839..34982384hg19UCSC Ensembl
Innerchr15:32530131..32769676hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38239546
hg19239546
hg18239546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569110
Supporting Variants
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv840369
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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