A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901826



Internal ID22676979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98783191..98809952hg38UCSC Ensembl
chr4:99704342..99731103hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3826762
hg1926762
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901826
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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