A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028434



Internal ID15534934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26865192..26977247hg38UCSC Ensembl
Innerchr5:26865301..26977354hg19UCSC Ensembl
Innerchr5:26901058..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 StatusS
Merged Variantsnsv597678
Supporting Variants
Samples
Known GenesCDH9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1028434
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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