A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847382



Internal ID16141338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77818881..77819750hg38UCSC Ensembl
Innerchr15:78111223..78112092hg19UCSC Ensembl
Innerchr15:75898278..75899147hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38870
hg19870
hg18870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570174
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv847382
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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