A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597607



Internal ID16385016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24522696..24592669hg38UCSC Ensembl
Innerchr5:24522805..24592778hg19UCSC Ensembl
Innerchr5:24558562..24628535hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3869974
hg1969974
hg1869974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1027971
Samples
Known GenesCDH10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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