A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5863n100



Internal ID20157479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181145984..181181605hg38UCSC Ensembl
chr5:180572984..180608605hg19UCSC Ensembl
chr5:180505590..180541211hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3835622
hg1935622
hg1835622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020707, nsv1024060
Samples
Known GenesOR2V2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5863n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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