A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153047



Internal ID15853281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:92672576..92718442hg38UCSC Ensembl
Innerchr5:92008283..92054149hg19UCSC Ensembl
Innerchr5:92034039..92079905hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3845867
hg1945867
hg1845867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598939
Supporting Variants
Samples1780854061_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153047
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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