A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677017



Internal ID9596436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172068156..172068734hg38UCSC Ensembl
Outerchr5:172068119..172068784hg38UCSC Ensembl
Innerchr5:171495160..171495738hg19UCSC Ensembl
Outerchr5:171495123..171495788hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5759362
SamplesNA20757
Known GenesSTK10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677017
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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