A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784909



Internal ID19163158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19010337..19048003hg38UCSC Ensembl
Innerchr13:19584477..19622143hg19UCSC Ensembl
Innerchr13:18482477..18520143hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3837667
hg1937667
hg1837667
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892296
Supporting Variants
Samples
Known GenesLINC00442
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784909
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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