A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012463



Internal ID21921806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14182686..14182748hg38UCSC Ensembl
chr9:14182685..14182747hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596734
Samples
Known GenesNFIB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012463
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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