A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474141



Internal ID22532035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8712482..8766759hg38UCSC Ensembl
chr16:8806339..8860616hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3854278
hg1954278
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872146
Supporting Variants
Samples
Known GenesABAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474141
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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