A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892703



Internal ID18836837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76569435..76787451hg38UCSC Ensembl
Outerchr2:76569435..76787451hg38UCSC Ensembl
Innerchr2:76796561..77014577hg19UCSC Ensembl
Outerchr2:76796561..77014577hg19UCSC Ensembl
Innerchr2:76650069..76868085hg18UCSC Ensembl
Outerchr2:76650069..76868085hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38218017
hg19218017
hg18218017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788560
Samples
Known GenesLRRTM4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892703
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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