A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443382



Internal ID21100935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96022650..96025515hg38UCSC Ensembl
chr9:98784932..98787797hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382866
hg192866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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