A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657659



Internal ID9923764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172802595..172809381hg38UCSC Ensembl
chr5:172229598..172236384hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg386787
hg196787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5889747
SamplesNA19059
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657659
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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