A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893705



Internal ID19184525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60254910..60533843hg38UCSC Ensembl
Outerchr3:60254910..60533843hg38UCSC Ensembl
Innerchr3:60240638..60519576hg19UCSC Ensembl
Outerchr3:60240638..60519576hg19UCSC Ensembl
Innerchr3:60215678..60494616hg18UCSC Ensembl
Outerchr3:60215678..60494616hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38278934
hg19278939
hg18278939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783030
Samples
Known GenesFHIT
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893705
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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