A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450979



Internal ID21108532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95602209..95602780hg38UCSC Ensembl
chr9:98364491..98365062hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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