A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786776



Internal ID19180470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:51295971..51327698hg38UCSC Ensembl
Innerchr14:51762689..51794416hg19UCSC Ensembl
Innerchr14:50832439..50864166hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3831728
hg1931728
hg1831728
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892543
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786776
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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