A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023673



Internal ID83496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35804004..35822928hg38UCSC Ensembl
chr9:35804001..35822925hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3818925
hg1918925
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560757
Supporting Variants
Samples
Known GenesFAM221B, HINT2, NPR2, SPAG8
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023673
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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