A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514065



Internal ID22572023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66891571..66893303hg38UCSC Ensembl
chr9:40799538..40801270hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381733
hg191733
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514065
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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