A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556871



Internal ID21881226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145554881..145556402hg38UCSC Ensembl
chr4:146476033..146477554hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381522
hg191522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995253
Supporting Variants
Samples
Known GenesSMAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556871
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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