A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511457



Internal ID22569409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128839640..128844925hg38UCSC Ensembl
chr9:131601919..131607204hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385286
hg195286
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859928
Supporting Variants
Samples
Known GenesCCBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511457
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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