A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893621



Internal ID18837755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2236385..2250335hg38UCSC Ensembl
Outerchr3:2236385..2250335hg38UCSC Ensembl
Innerchr3:2278069..2292019hg19UCSC Ensembl
Outerchr3:2278069..2292019hg19UCSC Ensembl
Innerchr3:2253069..2267019hg18UCSC Ensembl
Outerchr3:2253069..2267019hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3813951
hg1913951
hg1813951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780179
Samples
Known GenesCNTN4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893621
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