A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935031



Internal ID22710366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77974208..77974306hg38UCSC Ensembl
chr18:75686164..75686262hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400335
Samples
Known GenesLINC01029
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935031
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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