A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891053



Internal ID22666085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87058519..87191593hg38UCSC Ensembl
chr3:87107669..87240743hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg38133075
hg19133075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424041
Samples
Known GenesLINC00506
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891053
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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