A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498066



Internal ID22556000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65875868..65886883hg38UCSC Ensembl
chr5:65171696..65182711hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3811016
hg1911016
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498066
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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