A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452150



Internal ID21109703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66026701..66032200hg38UCSC Ensembl
chr9:42489130..42494635hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg385500
hg195506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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