A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668142



Internal ID9934247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128890284..128895550hg38UCSC Ensembl
chr10:130688548..130693814hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385267
hg195267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6487004
SamplesHG00328
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668142
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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