A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600185



Internal ID16387594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:162026079..162059049hg38UCSC Ensembl
Innerchr5:161453085..161486055hg19UCSC Ensembl
Innerchr5:161385663..161418633hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3832971
hg1932971
hg1832971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154010
SamplesHGDP00741
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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