A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656897



Internal ID9923002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70494857..70514668hg38UCSC Ensembl
chr13:71068989..71088800hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3819812
hg1919812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6222719, essv5712851, essv5932351
SamplesNA19404, NA19908, NA19663
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656897
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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