A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922323



Internal ID22697548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71264822..71274936hg38UCSC Ensembl
chr9:73879738..73889852hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3810115
hg1910115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922323
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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