A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992860



Internal ID21902203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196470215..196470288hg38UCSC Ensembl
chr3:196197086..196197159hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556752
Samples
Known GenesRNF168
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992860
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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