A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568924



Internal ID16356333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33983968..33985706hg38UCSC Ensembl
Innerchr15:34276169..34277907hg19UCSC Ensembl
Innerchr15:32063461..32065199hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381739
hg191739
hg181739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149585, nssv1149586
SamplesHGDP00281, HGDP00039
Known GenesAVEN, CHRM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568924
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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