A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913360



Internal ID22688576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73289408..73291760hg38UCSC Ensembl
chr11:73000453..73002805hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382353
hg192353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362888
Samples
Known GenesP2RY6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913360
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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