A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530061



Internal ID306057
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 StatusM
Merged Variants
Supporting Variantsnssv17711303
Samples
Known GenesNTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530061
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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