A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673016



Internal ID9939121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24315624..24318050hg38UCSC Ensembl
chr10:24604553..24606979hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382427
hg192427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5490048, essv5435478
SamplesHG00106, HG01171
Known GenesKIAA1217
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673016
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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