A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597680



Internal ID16038403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26875005..26977247hg38UCSC Ensembl
Innerchr5:26875114..26977354hg19UCSC Ensembl
Innerchr5:26910871..27013111hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38102243
hg19102241
hg18102241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9699n54
Supporting Variantsnssv1028435
Samples
Known GenesCDH9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597680
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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