A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447417



Internal ID21104970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89290758..89305856hg38UCSC Ensembl
chr9:91905673..91920771hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3815099
hg1915099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195510
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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