A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv847559



Internal ID15794829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82163886..82298744hg38UCSC Ensembl
Innerchr15:82456227..82591082hg19UCSC Ensembl
Innerchr15:80243282..80378137hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38134859
hg19134856
hg18134856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570245
Supporting Variants
Samples
Known GenesADAMTS7P1, EFTUD1, FAM154B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv847559
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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