A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004587



Internal ID21913930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94564525..94591108hg38UCSC Ensembl
chr9:97326807..97353390hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3826584
hg1926584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585555
Samples
Known GenesFBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004587
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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