A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737939



Internal ID20513904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104151375..104151968hg38UCSC Ensembl
chr3:103870219..103870812hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737939
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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