A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1043284



Internal ID15549784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150404851..150412774hg38UCSC Ensembl
Innerchr5:149784414..149792337hg19UCSC Ensembl
Innerchr5:149764607..149772530hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg387924
hg197924
hg187924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599958
Supporting Variants
Samples
Known GenesCD74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1043284
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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