A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892434



Internal ID19183254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100161230..100357200hg38UCSC Ensembl
Outerchr13:100160601..100371219hg38UCSC Ensembl
Innerchr13:100813484..101009454hg19UCSC Ensembl
Outerchr13:100812855..101023473hg19UCSC Ensembl
Innerchr13:99611485..99807455hg18UCSC Ensembl
Outerchr13:99610856..99821474hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38210619
hg19210619
hg18210619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796713, essv25779564, essv25785398
Samples
Known GenesPCCA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892434
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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