A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081391



Internal ID21990624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113901024..113901024hg38UCSC Ensembl
chr9:116663304..116663304hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582832
Samples
Known GenesZNF618
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081391
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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