A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599800



Internal ID16387209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:138469963..138479901hg38UCSC Ensembl
Innerchr5:137805652..137815590hg19UCSC Ensembl
Innerchr5:137833551..137843489hg18UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg389939
hg199939
hg189939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10088n54
Supporting Variantsnssv1042053, nssv1042052
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599800
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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