A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788915



Internal ID19175729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12858132..12903183hg38UCSC Ensembl
Innerchr4:12859756..12904807hg19UCSC Ensembl
Innerchr4:12468854..12513905hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3845052
hg1945052
hg1845052
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893884
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788915
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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