A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796617



Internal ID19159969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60807948..60827529hg38UCSC Ensembl
Innerchr3:60793653..60813190hg19UCSC Ensembl
Innerchr3:60768693..60788230hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3819582
hg1919538
hg1819538
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893709
Supporting Variants
Samples
Known GenesFHIT
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796617
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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