A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678096



Internal ID9944201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119773993..119780303hg38UCSC Ensembl
chr10:121533505..121539815hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg386311
hg196311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5593861, essv5702325
SamplesHG01198, NA18871
Known GenesINPP5F
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678096
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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