A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739377



Internal ID20515350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19004149..19004436hg38UCSC Ensembl
chr3:19045641..19045928hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739377
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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