A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546226



Internal ID21870581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40534817..40534887hg38UCSC Ensembl
chr4:40536834..40536904hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997297
Supporting Variants
Samples
Known GenesRBM47
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546226
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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