A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991176



Internal ID21900519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101807881..101807954hg38UCSC Ensembl
chr3:101526725..101526798hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553222
Samples
Known GenesNXPE3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991176
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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