A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099731



Internal ID22008964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32420114..32420114hg38UCSC Ensembl
chr9:32420112..32420112hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586059
Samples
Known GenesACO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099731
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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