A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712333



Internal ID135999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28159789..28159915hg38UCSC Ensembl
chr17:26486815..26486941hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515411
Supporting Variants
Samples
Known GenesNLK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712333
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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