A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542499



Internal ID21866854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80050936..80050936hg38UCSC Ensembl
chr4:80972090..80972090hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072050
Supporting Variants
Samples
Known GenesANTXR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542499
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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