A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673572



Internal ID9592991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110252129..110254981hg38UCSC Ensembl
Outerchr10:110252072..110255063hg38UCSC Ensembl
Innerchr10:112011887..112014739hg19UCSC Ensembl
Outerchr10:112011830..112014821hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382992
hg192992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5997094
SamplesNA19712
Known GenesMXI1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673572
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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