A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671177



Internal ID9937282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44496759..44498273hg38UCSC Ensembl
Outerchr3:44496722..44498323hg38UCSC Ensembl
Innerchr3:44538251..44539765hg19UCSC Ensembl
Outerchr3:44538214..44539815hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5713215
SamplesHG00329
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671177
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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