A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551423



Internal ID21875778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:90377354..90734762hg38UCSC Ensembl
chr4:91298505..91655913hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38357409
hg19357409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5998651
Supporting Variants
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551423
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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