A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539148



Internal ID21863503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55960954..55961789hg38UCSC Ensembl
chr4:56827120..56827955hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998009
Supporting Variants
Samples
Known GenesCEP135
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539148
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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