A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678365



Internal ID9944470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124923260..124924034hg38UCSC Ensembl
chr10:126611829..126612603hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6556893, essv6356249, essv5395921, essv6054086, essv6563929
SamplesNA19723, NA19172, NA19654, HG01190, NA19712
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678365
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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