A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598413



Internal ID16385822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:69010231..69024875hg38UCSC Ensembl
Innerchr5:68306058..68320702hg19UCSC Ensembl
Innerchr5:68341814..68356458hg18UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3814645
hg1914645
hg1814645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1034609
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598413
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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