A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1030365



Internal ID15883551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:54860441..54896995hg38UCSC Ensembl
Innerchr5:54156269..54192823hg19UCSC Ensembl
Innerchr5:54192026..54228580hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3836555
hg1936555
hg1836555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598179
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1030365
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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