A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231842



Internal ID20798882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62467001..62470400hg38UCSC Ensembl
chr9:46778302..46781701hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231842
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00297


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