A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514964



Internal ID22572923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97215601..97217319hg38UCSC Ensembl
chr9:99977883..99979601hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381719
hg191719
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867369
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514964
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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