A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991002



Internal ID21900345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113976863..113977039hg38UCSC Ensembl
chr3:113695710..113695886hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541278
Samples
Known GenesKIAA1407
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991002
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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