A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779907



Internal ID19160729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83705979..83759138hg38UCSC Ensembl
Innerchr14:84172323..84225482hg19UCSC Ensembl
Innerchr14:83242076..83295235hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3853160
hg1953160
hg1853160
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892567
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779907
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