A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568768



Internal ID16009491
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 StatusM
Merged Variantsdgv4428n54
Supporting Variantsnssv839496, nssv839498, nssv839497
Samples
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568768
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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