A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9560n54



Internal ID22777455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7169738..7200104hg38UCSC Ensembl
chr5:7169851..7200217hg19UCSC Ensembl
chr5:7222851..7253217hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3830367
hg1930367
hg1830367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596980, nsv596979
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9560n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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