A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235838



Internal ID20802878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135865734..135958903hg38UCSC Ensembl
chr9:138757580..138850749hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3893170
hg1993170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437874
Supporting Variants
Samples
Known GenesCAMSAP1, UBAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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