A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024211



Internal ID83877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67601387..67618387hg38UCSC Ensembl
chr9:44747977..46276908hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3817001
hg191528932
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433440
Supporting Variants
Samples
Known GenesFAM27A, FAM27C, FAM27E2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024211
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.200374


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