A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232967



Internal ID20800007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88306974..88362640hg38UCSC Ensembl
chr9:90921889..90977555hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3855667
hg1955667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232967
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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