A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004054



Internal ID21913397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113268819..113268886hg38UCSC Ensembl
chr9:116031099..116031166hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585434
Samples
Known GenesCDC26
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004054
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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