A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671626



Internal ID9937731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100169740..100173850hg38UCSC Ensembl
chr13:100821994..100826104hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384111
hg194111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6301682
SamplesNA19383
Known GenesPCCA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671626
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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