A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790578



Internal ID19180404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75196251..76010348hg38UCSC Ensembl
Innerchr3:75245402..76059499hg19UCSC Ensembl
Innerchr3:75328092..76142189hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38814098
hg19814098
hg18814098
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893725
Supporting Variants
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, MIR4444-1, ZNF717
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=111
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790578
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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