A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893514



Internal ID19184334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:181173718..181530618hg38UCSC Ensembl
Outerchr2:181173718..181530618hg38UCSC Ensembl
Innerchr2:182038445..182395345hg19UCSC Ensembl
Outerchr2:182038445..182395345hg19UCSC Ensembl
Innerchr2:181746690..182103590hg18UCSC Ensembl
Outerchr2:181746690..182103590hg18UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38356901
hg19356901
hg18356901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788896
Samples
Known GenesITGA4, MIR4437
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893514
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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