A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780876



Internal ID19173859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83080930..83105263hg38UCSC Ensembl
Innerchr3:83130081..83154414hg19UCSC Ensembl
Innerchr3:83212771..83237104hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3824334
hg1924334
hg1824334
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893730
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780876
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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