A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023018



Internal ID83051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61341035..61341118hg38UCSC Ensembl
chr9:40624076..40624159hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491483
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023018
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003122


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