A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622578



Internal ID21814625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58119961..58120017hg38UCSC Ensembl
chr16:58153865..58153921hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020655
Supporting Variants
Samples
Known GenesC16orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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