A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839496



Internal ID15786766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31064222..31092594hg38UCSC Ensembl
Innerchr15:31356425..31384797hg19UCSC Ensembl
Innerchr15:29143717..29172089hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3828373
hg1928373
hg1828373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568768
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)nssv839496
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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