A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597608



Internal ID16385017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24539164..24568209hg38UCSC Ensembl
Innerchr5:24539273..24568318hg19UCSC Ensembl
Innerchr5:24575030..24604075hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3829046
hg1929046
hg1829046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1027972
Samples
Known GenesCDH10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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