A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545961



Internal ID15986684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32566811..32685350hg38UCSC Ensembl
Innerchr1:33032412..33150951hg19UCSC Ensembl
Innerchr1:32804999..32923538hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38118540
hg19118540
hg18118540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173811
SamplesHGDP00017
Known GenesRBBP4, SYNC, ZBTB8A, ZBTB8OS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545961
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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