A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513755



Internal ID22571711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5978128..5979145hg38UCSC Ensembl
chr9:5978128..5979145hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381018
hg191018
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858928
Supporting Variants
Samples
Known GenesKIAA2026
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513755
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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