A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476260



Internal ID22534158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14343749..14358498hg38UCSC Ensembl
chr16:14437606..14452355hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3814750
hg1914750
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881111
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476260
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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