A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221889



Internal ID20788929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63349601..63394700hg38UCSC Ensembl
chr9:67304573..67349672hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3845100
hg1945100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00302


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