A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633412



Internal ID7020221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104020468..104031294hg38UCSC Ensembl
Innerchr13:104020484..104031278hg38UCSC Ensembl
Outerchr13:104020452..104031310hg38UCSC Ensembl
chr13:104672818..104683644hg19UCSC Ensembl
Innerchr13:104672834..104683628hg19UCSC Ensembl
Outerchr13:104672802..104683660hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3810827
hg1910827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14886266, essv14886267
SamplesNA20356, HG03304
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633412
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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