A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569685



Internal ID16357094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62414416..62415506hg38UCSC Ensembl
Innerchr15:62706615..62707705hg19UCSC Ensembl
Innerchr15:60493907..60494997hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381091
hg191091
hg181091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4568n54
Supporting Variantsnssv843931, nssv843930, nssv843929
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569685
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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