A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953095



Internal ID22728391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187795390..187795390hg38UCSC Ensembl
chr3:187513178..187513178hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953095
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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