A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677862



Internal ID9943967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179039027..179046614hg38UCSC Ensembl
Outerchr5:179038990..179046664hg38UCSC Ensembl
Innerchr5:178466028..178473615hg19UCSC Ensembl
Outerchr5:178465991..178473665hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387675
hg197675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5867401
SamplesNA18941
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677862
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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