A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463381



Internal ID22521267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66166394..66171745hg38UCSC Ensembl
chr11:65933865..65939216hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385352
hg195352
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847694
Supporting Variants
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463381
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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