A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672894



Internal ID9592313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30034491..30043476hg38UCSC Ensembl
chr10:30323420..30332405hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg388986
hg198986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5784037
SamplesNA12830
Known GenesKIAA1462
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672894
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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