A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9699n54



Internal ID20143123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26865192..26977247hg38UCSC Ensembl
chr5:26865301..26977354hg19UCSC Ensembl
chr5:26901058..27013111hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38112056
hg19112054
hg18112054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597680, nsv597678
Samples
Known GenesCDH9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9699n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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