A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544100



Internal ID21868455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40201457..40212735hg38UCSC Ensembl
chr4:40203077..40214355hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3811279
hg1911279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997261
Supporting Variants
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544100
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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