A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9880n54



Internal ID22777775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75052851..75053675hg38UCSC Ensembl
chr5:74348676..74349500hg19UCSC Ensembl
chr5:74384432..74385256hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38825
hg19825
hg18825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598658, nsv598668, nsv598667, nsv598665, nsv598663, nsv598661, nsv598662, nsv598657, nsv598656
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9880n54
Frequency
Sample Size17421
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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