A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438544



Internal ID21096097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136265514..136322414hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3856901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438544
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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