A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479093



Internal ID22536995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71518439..71521141hg38UCSC Ensembl
chr16:71552342..71555044hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479093
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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