A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420732



Internal ID22478602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184697354..184697425hg38UCSC Ensembl
chr4:185618508..185618579hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906975
Supporting Variants
Samples
Known GenesCENPU
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420732
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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