A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438850



Internal ID22496720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99903540..99903617hg38UCSC Ensembl
chr9:102665822..102665899hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909366
Supporting Variants
Samples
Known GenesLOC441461
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438850
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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