A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992414



Internal ID21901757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185354190..185354275hg38UCSC Ensembl
chr3:185071978..185072063hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543979
Samples
Known GenesMAP3K13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992414
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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