A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5544893



Internal ID9712941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65169651..65171360hg38UCSC Ensembl
chr15:65461989..65463698hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381710
hg191710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670622
Supporting Variants
SamplesNA19466
Known GenesCLPX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5544893
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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