A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631579



Internal ID7018388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25354760..25367875hg38UCSC Ensembl
Innerchr13:25354761..25367874hg38UCSC Ensembl
Outerchr13:25354759..25367876hg38UCSC Ensembl
chr13:25928898..25942013hg19UCSC Ensembl
Innerchr13:25928899..25942012hg19UCSC Ensembl
Outerchr13:25928897..25942014hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3813116
hg1913116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14672899, essv14672898, essv14672900, essv14672897
SamplesNA19625, HG02799, HG02721, NA19312
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631579
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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