A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890688



Internal ID19184990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103374111..103417514hg38UCSC Ensembl
Outerchr5:103374111..103417514hg38UCSC Ensembl
Innerchr5:102709812..102753215hg19UCSC Ensembl
Outerchr5:102709812..102753215hg19UCSC Ensembl
Innerchr5:102737711..102781114hg18UCSC Ensembl
Outerchr5:102737711..102781114hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3843404
hg1943404
hg1843404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796790
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890688
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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