A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9582n54



Internal ID22777477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10760904..10761497hg38UCSC Ensembl
chr5:10761016..10761609hg19UCSC Ensembl
chr5:10814016..10814609hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38594
hg19594
hg18594
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597140, nsv597141
Samples
Known GenesDAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9582n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss4
Observed Complex0
Frequencyn/a


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