A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788896



Internal ID18816460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:181173718..181530618hg38UCSC Ensembl
Innerchr2:182038445..182395345hg19UCSC Ensembl
Innerchr2:181746690..182103590hg18UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38356901
hg19356901
hg18356901
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893514
Supporting Variants
Samples
Known GenesITGA4, MIR4437
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=65
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788896
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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