A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711303



Internal ID134969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9021586..9021674hg38UCSC Ensembl
chr17:8924903..8924991hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530061
Supporting Variants
Samples
Known GenesNTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711303
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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