A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893702



Internal ID18837836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58557785..58858605hg38UCSC Ensembl
Outerchr3:58557785..58858605hg38UCSC Ensembl
Innerchr3:58543512..58844331hg19UCSC Ensembl
Outerchr3:58543512..58844331hg19UCSC Ensembl
Innerchr3:58518552..58819371hg18UCSC Ensembl
Outerchr3:58518552..58819371hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38300821
hg19300820
hg18300820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796600
Samples
Known GenesC3orf67, FAM107A, FAM3D
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893702
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer