A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572363



Internal ID21764406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150366628..150366954hg38UCSC Ensembl
chr5:149746191..149746517hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007886
Supporting Variants
Samples
Known GenesTCOF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572363
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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