A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631871



Internal ID7018680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41287884..41299437hg38UCSC Ensembl
Innerchr13:41287931..41299390hg38UCSC Ensembl
Outerchr13:41287837..41299484hg38UCSC Ensembl
chr13:41862020..41873573hg19UCSC Ensembl
Innerchr13:41862067..41873526hg19UCSC Ensembl
Outerchr13:41861973..41873620hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3811554
hg1911554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14704725
SamplesNA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631871
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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