A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423907



Internal ID22481777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26415268..26415319hg38UCSC Ensembl
chr4:26416890..26416941hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904653
Supporting Variants
Samples
Known GenesRBPJ
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423907
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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