A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5887884



Internal ID8865287
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 StatusS
Merged Variantsesv2661625
Supporting Variants
SamplesNA19722
Known GenesOIP5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5887884
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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