A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478307



Internal ID22536208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31539970..31543309hg38UCSC Ensembl
chr16:31551291..31554630hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383340
hg193340
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478307
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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