A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995027



Internal ID21904370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96069124..96069183hg38UCSC Ensembl
chr3:95787968..95788027hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995027
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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