A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954432



Internal ID22729676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62884995..62884995hg38UCSC Ensembl
chr9:66540819..66540819hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954432
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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