A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796190



Internal ID19169467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55992201..56201010hg38UCSC Ensembl
Innerchr13:56566335..56775144hg19UCSC Ensembl
Innerchr13:55464336..55673145hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38208810
hg19208810
hg18208810
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892351
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796190
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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