A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893993



Internal ID19184847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:94127972..94169127hg38UCSC Ensembl
Outerchr4:94127972..94169127hg38UCSC Ensembl
Innerchr4:95049123..95090278hg19UCSC Ensembl
Outerchr4:95049123..95090278hg19UCSC Ensembl
Innerchr4:95268146..95309301hg18UCSC Ensembl
Outerchr4:95268146..95309301hg18UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3841156
hg1941156
hg1841156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779265, essv25778485
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893993
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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