A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890684



Internal ID19184986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101683566..101905574hg38UCSC Ensembl
Outerchr5:101589980..101996595hg38UCSC Ensembl
Innerchr5:101019270..101241278hg19UCSC Ensembl
Outerchr5:100925684..101332299hg19UCSC Ensembl
Innerchr5:101047169..101269177hg18UCSC Ensembl
Outerchr5:100953583..101360198hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38406616
hg19406616
hg18406616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792953, essv25791872, essv25790941, essv25792526, essv25789972
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890684
Frequency
Sample Size3017
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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