A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453051



Internal ID22510924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61482102..61483293hg38UCSC Ensembl
chr11:61249574..61250765hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852932
Supporting Variants
Samples
Known GenesPPP1R32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453051
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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