A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893886



Internal ID18838020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15963240..16107473hg38UCSC Ensembl
Outerchr4:15963240..16107473hg38UCSC Ensembl
Innerchr4:15964863..16109096hg19UCSC Ensembl
Outerchr4:15964863..16109096hg19UCSC Ensembl
Innerchr4:15573961..15718194hg18UCSC Ensembl
Outerchr4:15573961..15718194hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38144234
hg19144234
hg18144234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785400
Samples
Known GenesPROM1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893886
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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