A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537624



Internal ID21861979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2496472..2496472hg38UCSC Ensembl
chr4:2498199..2498199hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382567
hg192567
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064860
Supporting Variants
Samples
Known GenesRNF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537624
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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