A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801630



Internal ID19163084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62185502..62252165hg38UCSC Ensembl
Innerchr14:62652220..62718883hg19UCSC Ensembl
Innerchr14:61721973..61788636hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3866664
hg1966664
hg1866664
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892554
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801630
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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