A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894027



Internal ID19184881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:127985398..128001851hg38UCSC Ensembl
Outerchr4:127985398..128001851hg38UCSC Ensembl
Innerchr4:128906553..128923006hg19UCSC Ensembl
Outerchr4:128906553..128923006hg19UCSC Ensembl
Innerchr4:129126003..129142456hg18UCSC Ensembl
Outerchr4:129126003..129142456hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3816454
hg1916454
hg1816454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796105
Samples
Known GenesC4orf29
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894027
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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