A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890690



Internal ID19184992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103748433..104198183hg38UCSC Ensembl
Outerchr5:103748433..104198183hg38UCSC Ensembl
Innerchr5:103084134..103533884hg19UCSC Ensembl
Outerchr5:103084134..103533884hg19UCSC Ensembl
Innerchr5:103112033..103561783hg18UCSC Ensembl
Outerchr5:103112033..103561783hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg38449751
hg19449751
hg18449751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790439
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890690
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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