A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661625



Internal ID9581044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41322756..41325983hg38UCSC Ensembl
chr15:41614954..41618181hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg383228
hg193228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5887884
SamplesNA19722
Known GenesOIP5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661625
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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