A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229143



Internal ID20796183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137992197..138061476hg38UCSC Ensembl
chr9:140886649..140955928hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3869280
hg1969280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438332
Supporting Variants
Samples
Known GenesCACNA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229143
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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