A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5691n100



Internal ID22791778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62729697..63580003hg38UCSC Ensembl
chr5:62025524..62875830hg19UCSC Ensembl
chr5:62061280..62911586hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38850307
hg19850307
hg18850307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033401, nsv1035049, nsv1022825
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)dgv5691n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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