A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513015



Internal ID22570970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35261155..35263958hg38UCSC Ensembl
chr9:35261152..35263955hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382804
hg192804
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856704
Supporting Variants
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513015
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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