A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711273



Internal ID134939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8379611..8379683hg38UCSC Ensembl
chr17:8282929..8283001hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516696
Supporting Variants
Samples
Known GenesRPL26
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711273
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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