A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022983



Internal ID83022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39444000..39617000hg38UCSC Ensembl
chr9:41589018..41762018hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38173001
hg19173001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142142
Supporting Variants
Samples
Known GenesLOC653501, ZNF658B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022983
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.184485


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