A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724672



Internal ID148338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49846029..49847822hg38UCSC Ensembl
chr17:47923391..47925184hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381794
hg191794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531534
Supporting Variants
Samples
Known GenesFLJ45513, TAC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724672
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004237


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