A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782033



Internal ID19180122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88321158..88372044hg38UCSC Ensembl
Innerchr13:88973413..89024299hg19UCSC Ensembl
Innerchr13:87771414..87822300hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3850887
hg1950887
hg1850887
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892416
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782033
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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