A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445516



Internal ID21103069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94633950..94639360hg38UCSC Ensembl
chr9:97396232..97401642hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385411
hg195411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178447
Samples
Known GenesFBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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