A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956830



Internal ID22731986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69762322..69762322hg38UCSC Ensembl
chr9:72377238..72377238hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956830
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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