A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597885



Internal ID16385294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42019008..42192518hg38UCSC Ensembl
Innerchr5:42019110..42192620hg19UCSC Ensembl
Innerchr5:42054867..42228377hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38173511
hg19173511
hg18173511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153346
Samples1782681195_A
Known GenesLOC101926960
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597885
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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