A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632971



Internal ID7019781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85219561..85253818hg38UCSC Ensembl
chr13:85793696..85827953hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3834258
hg1934258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv358e214
Supporting Variantsessv14822808, essv14822810, essv14822809
SamplesNA19648, NA20535, HG03755
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632971
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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