A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955422



Internal ID22730624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13424322..13424322hg38UCSC Ensembl
chr9:13424321..13424321hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437765
Samples
Known GenesFLJ41200
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955422
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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