A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010951



Internal ID21920294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:293723..686362hg38UCSC Ensembl
chr9:293723..686362hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38392640
hg19392640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577744
Samples
Known GenesDOCK8, KANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010951
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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