A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551164



Internal ID21875519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26360918..26360918hg38UCSC Ensembl
chr4:26362540..26362540hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070068
Supporting Variants
Samples
Known GenesRBPJ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551164
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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