A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892350



Internal ID19183170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55256812..55310133hg38UCSC Ensembl
Outerchr13:55256812..55310133hg38UCSC Ensembl
Innerchr13:55830947..55884268hg19UCSC Ensembl
Outerchr13:55830947..55884268hg19UCSC Ensembl
Innerchr13:54728948..54782269hg18UCSC Ensembl
Outerchr13:54728948..54782269hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3853322
hg1953322
hg1853322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782130
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892350
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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