A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632929



Internal ID7019740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83892485..84089073hg38UCSC Ensembl
chr13:84466620..84663208hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38196589
hg19196589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14822359, essv14822360, essv14822358
SamplesNA12889, HG01362, HG02351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632929
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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