A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438419



Internal ID22496289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70383197..70383264hg38UCSC Ensembl
chr9:72998113..72998180hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438419
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010


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