A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597084



Internal ID16384493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9896051..9928750hg38UCSC Ensembl
Innerchr5:9896163..9928862hg19UCSC Ensembl
Innerchr5:9949163..9981862hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3832700
hg1932700
hg1832700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9574n54
Supporting Variantsnssv1153011
SamplesHGDP00667
Known GenesLOC285692
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597084
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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