A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568723



Internal ID16009446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30194842..30467578hg38UCSC Ensembl
Innerchr15:30487045..30759781hg19UCSC Ensembl
Innerchr15:28274337..28547073hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38272737
hg19272737
hg18272737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4419n54
Supporting Variantsnssv839449
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568723
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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