A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892351



Internal ID19183171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55994164..56201010hg38UCSC Ensembl
Outerchr13:55992201..56205759hg38UCSC Ensembl
Innerchr13:56568298..56775144hg19UCSC Ensembl
Outerchr13:56566335..56779893hg19UCSC Ensembl
Innerchr13:55466299..55673145hg18UCSC Ensembl
Outerchr13:55464336..55677894hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38213559
hg19213559
hg18213559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787263, essv25796190
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892351
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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