A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662972



Internal ID9929077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73051175..73053083hg38UCSC Ensembl
chr4:73916892..73918800hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381909
hg191909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5525482
SamplesNA19394
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662972
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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