A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893709



Internal ID19184529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60807948..60827529hg38UCSC Ensembl
Outerchr3:60801895..60827530hg38UCSC Ensembl
Innerchr3:60793653..60813190hg19UCSC Ensembl
Outerchr3:60787599..60813191hg19UCSC Ensembl
Innerchr3:60768693..60788230hg18UCSC Ensembl
Outerchr3:60762639..60788231hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3825636
hg1925593
hg1825593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780686, essv25781062, essv25796617
Samples
Known GenesFHIT
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893709
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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