A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782276



Internal ID19178311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183983359..184005289hg38UCSC Ensembl
Innerchr3:183701147..183723077hg19UCSC Ensembl
Innerchr3:185183841..185205771hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3821931
hg1921931
hg1821931
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893835
Supporting Variants
Samples
Known GenesABCC5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782276
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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