A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890670



Internal ID18838286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90583442..91314051hg38UCSC Ensembl
Outerchr5:90583442..91324492hg38UCSC Ensembl
Innerchr5:89879259..90609868hg19UCSC Ensembl
Outerchr5:89879259..90620309hg19UCSC Ensembl
Innerchr5:89915015..90645624hg18UCSC Ensembl
Outerchr5:89915015..90656065hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38741051
hg19741051
hg18741051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789304, essv25791541
Samples
Known GenesGPR98, LUCAT1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890670
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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