A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153584



Internal ID15877434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113740398..113845592hg38UCSC Ensembl
Innerchr5:113076095..113181289hg19UCSC Ensembl
Innerchr5:113103994..113209188hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38105195
hg19105195
hg18105195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599408
Supporting Variants
SamplesHGDP00991
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153584
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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