A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891925



Internal ID18839635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7598031..7693943hg38UCSC Ensembl
Outerchr11:7596802..7700323hg38UCSC Ensembl
Innerchr11:7619262..7715174hg19UCSC Ensembl
Outerchr11:7618033..7721870hg19UCSC Ensembl
Innerchr11:7575838..7671750hg18UCSC Ensembl
Outerchr11:7574609..7678446hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38103522
hg19103838
hg18103838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789192, essv25791130, essv25791421
Samples
Known GenesCYB5R2, OVCH2, PPFIBP2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891925
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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