A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995981



Internal ID21905324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169229924..169230059hg38UCSC Ensembl
chr4:170151075..170151210hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548444
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995981
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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