A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955435



Internal ID22730637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97075628..97075628hg38UCSC Ensembl
chr9:99837910..99837910hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955435
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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