A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5961378



Internal ID9682711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121010188..121027998hg38UCSC Ensembl
chr10:122769701..122787511hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3817811
hg1917811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662007
Supporting Variants
SamplesNA19434
Known GenesMIR5694
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5961378
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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