A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588621



Internal ID21780664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128833732..128833732hg38UCSC Ensembl
chr9:131596011..131596011hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091973
Supporting Variants
Samples
Known GenesCCBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588621
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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