A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597852



Internal ID16038575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:37839783..37840305hg38UCSC Ensembl
Innerchr5:37839885..37840407hg19UCSC Ensembl
Innerchr5:37875642..37876164hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38523
hg19523
hg18523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9728n54
Supporting Variantsnssv1029098
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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