A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1044497



Internal ID15897683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:159467341..159471498hg38UCSC Ensembl
Innerchr5:158894349..158898506hg19UCSC Ensembl
Innerchr5:158826927..158831084hg18UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg384158
hg194158
hg184158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600135
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)nssv1044497
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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