A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676235



Internal ID9942340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:174560394..174569316hg38UCSC Ensembl
Outerchr5:174560237..174569469hg38UCSC Ensembl
Innerchr5:173987397..173996319hg19UCSC Ensembl
Outerchr5:173987240..173996472hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg389233
hg199233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5928642
SamplesHG00137
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676235
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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