A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221611



Internal ID20788651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35210597..35355016hg38UCSC Ensembl
chr9:35210594..35355013hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38144420
hg19144420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453341
Supporting Variants
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221611
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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