A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5796n100



Internal ID22791883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120125101..120176151hg38UCSC Ensembl
chr5:119460796..119511846hg19UCSC Ensembl
chr5:119488695..119539745hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3851051
hg1951051
hg1851051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018247, nsv1016024
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5796n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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