A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712335



Internal ID136001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28186902..28186990hg38UCSC Ensembl
chr17:26513928..26514016hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519210
Supporting Variants
Samples
Known GenesNLK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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