A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839495



Internal ID15786765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31064222..31085370hg38UCSC Ensembl
Innerchr15:31356425..31377573hg19UCSC Ensembl
Innerchr15:29143717..29164865hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3821149
hg1921149
hg1821149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568767
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)nssv839495
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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