A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462055



Internal ID22519940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110041758..110047305hg38UCSC Ensembl
chr13:110694105..110699652hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385548
hg195548
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462055
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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