A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594641



Internal ID21786684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42454740..42458740hg38UCSC Ensembl
chr9:44512379..44516379hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018492
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594641
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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