A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893710



Internal ID19184530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60871271..61096095hg38UCSC Ensembl
Outerchr3:60871271..61096095hg38UCSC Ensembl
Innerchr3:60856943..61081768hg19UCSC Ensembl
Outerchr3:60856943..61081768hg19UCSC Ensembl
Innerchr3:60831983..61056808hg18UCSC Ensembl
Outerchr3:60831983..61056808hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38224825
hg19224826
hg18224826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781497
Samples
Known GenesFHIT
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893710
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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