A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600391



Internal ID16387800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178061280..178122490hg38UCSC Ensembl
Innerchr5:177488281..177549491hg19UCSC Ensembl
Innerchr5:177420887..177482097hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3861211
hg1961211
hg1861211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1045761
Samples
Known GenesN4BP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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