A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568722



Internal ID16356131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30194842..30389978hg38UCSC Ensembl
Innerchr15:30487045..30682181hg19UCSC Ensembl
Innerchr15:28274337..28469473hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38195137
hg19195137
hg18195137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4418n54
Supporting Variantsnssv839448
Samples
Known GenesCHRFAM7A, DKFZP434L187
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568722
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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