A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923485



Internal ID22698712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131742356..131746874hg38UCSC Ensembl
chr9:134617743..134622261hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg384519
hg194519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923485
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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