A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949355



Internal ID22724805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180407488..180407488hg38UCSC Ensembl
chr3:180125276..180125276hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949355
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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