A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749801



Internal ID20525835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167126818..167131495hg38UCSC Ensembl
chr3:166844606..166849283hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg384678
hg194678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749801
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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