A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597699



Internal ID16385108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27770447..28261854hg38UCSC Ensembl
Innerchr5:27770554..28261961hg19UCSC Ensembl
Innerchr5:27806311..28297718hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38491408
hg19491408
hg18491408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9703n54
Supporting Variantsnssv1028690
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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