A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468953



Internal ID22526843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:22184883..22187177hg38UCSC Ensembl
chr13:22759022..22761316hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382295
hg192295
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854066
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468953
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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