A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799713



Internal ID19181867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103201980..103239505hg38UCSC Ensembl
Innerchr14:103668317..103705842hg19UCSC Ensembl
Innerchr14:102738070..102775595hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3837526
hg1937526
hg1837526
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892580
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799713
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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