A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465317



Internal ID22523206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63607599..63614765hg38UCSC Ensembl
chr11:63375071..63382237hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg387167
hg197167
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856831
Supporting Variants
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465317
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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