A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839499



Internal ID15786769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31064222..31101271hg38UCSC Ensembl
Innerchr15:31356425..31393474hg19UCSC Ensembl
Innerchr15:29143717..29180766hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3837050
hg1937050
hg1837050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568769
Supporting Variants
Samples
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839499
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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