A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958300



Internal ID22733374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35516022..35516022hg38UCSC Ensembl
chr9:35516019..35516019hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449507
Samples
Known GenesRUSC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958300
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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