A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892778



Internal ID18836912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6977718..7336522hg38UCSC Ensembl
Outerchr16:6977718..7336522hg38UCSC Ensembl
Innerchr16:7027719..7386523hg19UCSC Ensembl
Outerchr16:7027719..7386523hg19UCSC Ensembl
Innerchr16:6967720..7326524hg18UCSC Ensembl
Outerchr16:6967720..7326524hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38358805
hg19358805
hg18358805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786200
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892778
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