A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362888



Internal ID22588557
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 StatusS
Merged Variantsnsv5913360
Supporting Variants
Samples
Known GenesP2RY6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362888
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer