A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907735



Internal ID22682945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91022410..91028893hg38UCSC Ensembl
chr9:93784692..93791175hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg386484
hg196484
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907735
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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