A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967337



Internal ID22742272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118593734..118593734hg38UCSC Ensembl
chr9:121356012..121356012hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967337
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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