A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599929



Internal ID16387338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:145206960..145275484hg38UCSC Ensembl
Innerchr5:144586523..144655047hg19UCSC Ensembl
Innerchr5:144566716..144635240hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3868525
hg1968525
hg1868525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153599
Samples1780862380_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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