A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510665



Internal ID22568616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107917526..107919825hg38UCSC Ensembl
chr9:110679807..110682106hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510665
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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