A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998651



Internal ID21907994
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 StatusM
Merged Variants
Supporting Variantsnssv17551423
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998651
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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