A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631870



Internal ID7018679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41275996..41287087hg38UCSC Ensembl
Innerchr13:41276007..41287076hg38UCSC Ensembl
Outerchr13:41275985..41287098hg38UCSC Ensembl
chr13:41850132..41861223hg19UCSC Ensembl
Innerchr13:41850143..41861212hg19UCSC Ensembl
Outerchr13:41850121..41861234hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3811092
hg1911092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14704724
SamplesHG02429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631870
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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