A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898640



Internal ID22673758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67701686..67707661hg38UCSC Ensembl
chr4:68567404..68573379hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg385976
hg195976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426061
Samples
Known GenesUBA6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898640
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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