A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994133



Internal ID21903476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51694006..51694096hg38UCSC Ensembl
chr3:51728022..51728112hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545614
Samples
Known GenesTEX264
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994133
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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