A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791992



Internal ID19181788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32427020..32651890hg38UCSC Ensembl
Innerchr4:32428642..32653512hg19UCSC Ensembl
Innerchr4:32072540..32297410hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38224871
hg19224871
hg18224871
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893907
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=60
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791992
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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