A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9907n54



Internal ID22777802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84487481..84611836hg38UCSC Ensembl
chr5:83783299..83907654hg19UCSC Ensembl
chr5:83819055..83943410hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38124356
hg19124356
hg18124356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598788, nsv598787
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9907n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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