A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781440



Internal ID18814473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44070887..44660661hg38UCSC Ensembl
Innerchr14:44540090..45129864hg19UCSC Ensembl
Innerchr14:43609840..44199614hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38589775
hg19589775
hg18589775
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892524
Supporting Variants
Samples
Known GenesFSCB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=137
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781440
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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