A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711259



Internal ID134925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8281755..8283054hg38UCSC Ensembl
chr17:8185073..8186372hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711259
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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