A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5997094



Internal ID8974497
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 StatusS
Merged Variantsesv2673572
Supporting Variants
SamplesNA19712
Known GenesMXI1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5997094
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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