A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568721



Internal ID16356130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30194842..30382181hg38UCSC Ensembl
Innerchr15:30487045..30674384hg19UCSC Ensembl
Innerchr15:28274337..28461676hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38187340
hg19187340
hg18187340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4418n54
Supporting Variantsnssv839447
Samples
Known GenesCHRFAM7A, DKFZP434L187
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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