A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460855



Internal ID22518738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99189101..99193105hg38UCSC Ensembl
chr13:99841355..99845359hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384005
hg194005
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460855
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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