A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893984



Internal ID19184838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90653225..90686212hg38UCSC Ensembl
Outerchr4:90653225..90686212hg38UCSC Ensembl
Innerchr4:91574376..91607363hg19UCSC Ensembl
Outerchr4:91574376..91607363hg19UCSC Ensembl
Innerchr4:91793399..91826386hg18UCSC Ensembl
Outerchr4:91793399..91826386hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3832988
hg1932988
hg1832988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782111
Samples
Known GenesCCSER1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893984
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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