A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023672



Internal ID83495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35804000..35822000hg38UCSC Ensembl
chr9:35803997..35821997hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142595
Supporting Variants
Samples
Known GenesFAM221B, HINT2, NPR2, SPAG8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023672
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00047


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