A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657868



Internal ID9923973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96061027..96069361hg38UCSC Ensembl
chr14:96527364..96535698hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388335
hg198335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6090544
SamplesNA19190
Known GenesC14orf132
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657868
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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