A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226511



Internal ID20793551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137573823..137576646hg38UCSC Ensembl
chr9:140468275..140471098hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382824
hg192824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438076
Supporting Variants
Samples
Known GenesDPH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226511
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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