A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024142



Internal ID83821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66229191..66245191hg38UCSC Ensembl
chr9:42276019..42292022hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3816001
hg1916004
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415150
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024142
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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