A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783030



Internal ID19161667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60254910..60533843hg38UCSC Ensembl
Innerchr3:60240638..60519576hg19UCSC Ensembl
Innerchr3:60215678..60494616hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38278934
hg19278939
hg18278939
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893705
Supporting Variants
Samples
Known GenesFHIT
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=133
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783030
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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