A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539464



Internal ID21863819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167787870..167846007hg38UCSC Ensembl
chr4:168709021..168767158hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3858138
hg1958138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539464
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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