A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021884



Internal ID82246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22702573..22736779hg38UCSC Ensembl
chr9:22702572..22736778hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3834207
hg1934207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474588
Supporting Variants
Samples
Known GenesFLJ35282
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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