A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782111



Internal ID19167611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90653225..90686212hg38UCSC Ensembl
Innerchr4:91574376..91607363hg19UCSC Ensembl
Innerchr4:91793399..91826386hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3832988
hg1932988
hg1832988
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893984
Supporting Variants
Samples
Known GenesCCSER1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782111
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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