A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14735071



Internal ID5691367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:55324474..55468206hg38UCSC Ensembl
Innerchr13:55324505..55468175hg38UCSC Ensembl
Outerchr13:55324443..55468237hg38UCSC Ensembl
chr13:55898609..56042341hg19UCSC Ensembl
Innerchr13:55898640..56042310hg19UCSC Ensembl
Outerchr13:55898578..56042372hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38143733
hg19143733
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3632155
Supporting Variants
SamplesNA19085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14735071
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer