A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602378



Internal ID21794425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2546092..2650196hg38UCSC Ensembl
chr16:2596093..2700197hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38104105
hg19104105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108817
Supporting Variants
Samples
Known GenesFLJ42627, LOC652276, PDPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602378
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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