A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550816



Internal ID21875171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71742704..71744189hg38UCSC Ensembl
chr4:72608421..72609906hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381486
hg191486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998072
Supporting Variants
Samples
Known GenesGC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550816
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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