A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893907



Internal ID19184761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32427020..32651890hg38UCSC Ensembl
Outerchr4:32427020..32651890hg38UCSC Ensembl
Innerchr4:32428642..32653512hg19UCSC Ensembl
Outerchr4:32428642..32653512hg19UCSC Ensembl
Innerchr4:32072540..32297410hg18UCSC Ensembl
Outerchr4:32072540..32297410hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38224871
hg19224871
hg18224871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791992
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893907
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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