A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667952



Internal ID9934057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173538897..173545293hg38UCSC Ensembl
chr5:172965900..172972296hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg386397
hg196397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5942001
SamplesNA19783
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667952
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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