A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454773



Internal ID21112326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62896801..62929400hg38UCSC Ensembl
chr9:66552625..66585224hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3832600
hg1932600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454773
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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