A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672546



Internal ID9938651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101685977..101686578hg38UCSC Ensembl
chr10:103445734..103446335hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6191274, essv6178211
SamplesHG00254, NA20786
Known GenesFBXW4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672546
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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