A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707580



Internal ID131246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26090303..26101955hg38UCSC Ensembl
chr16:26101624..26113276hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3811653
hg1911653
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147200
Supporting Variants
Samples
Known GenesHS3ST4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707580
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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