A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798171



Internal ID19168727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83960759..84050777hg38UCSC Ensembl
Innerchr13:84534894..84624912hg19UCSC Ensembl
Innerchr13:83432895..83522913hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3890019
hg1990019
hg1890019
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892406
Supporting Variants
Samples
Known GenesMIR548F1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798171
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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