A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597327



Internal ID16384736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17352298..17356057hg38UCSC Ensembl
Innerchr5:17352407..17356166hg19UCSC Ensembl
Innerchr5:17405407..17409166hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg383760
hg193760
hg183760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9624n54
Supporting Variantsnssv1026342, nssv1026341
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597327
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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