A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610590



Internal ID21802637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1075998..1075998hg38UCSC Ensembl
chr16:1125998..1125998hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083929
Supporting Variants
Samples
Known GenesSSTR5, SSTR5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610590
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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