A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9879n54



Internal ID22777774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75052851..75053542hg38UCSC Ensembl
chr5:74348676..74349367hg19UCSC Ensembl
chr5:74384432..74385123hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38692
hg19692
hg18692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598655, nsv598660, nsv598664
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9879n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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