A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710111



Internal ID133777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64909620..64909792hg38UCSC Ensembl
chr16:64943523..64943695hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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