A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001260



Internal ID21910603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105627552..105627621hg38UCSC Ensembl
chr9:108389833..108389902hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596662
Samples
Known GenesFKTN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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