A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600090



Internal ID16040813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:154665720..154686645hg38UCSC Ensembl
Innerchr5:154045280..154066205hg19UCSC Ensembl
Innerchr5:154025473..154046398hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3820926
hg1920926
hg1820926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153374
Samples1782681296_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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