A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569815



Internal ID16357224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70249681..70305902hg38UCSC Ensembl
Innerchr15:70542020..70598241hg19UCSC Ensembl
Innerchr15:68329074..68385295hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3856222
hg1956222
hg1856222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4585n54
Supporting Variantsnssv1149239
SamplesHGDP00465
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569815
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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