A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840080



Internal ID22615015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67701683..67707834hg38UCSC Ensembl
chr4:68567401..68573552hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg386152
hg196152
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490469
Samples
Known GenesUBA6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840080
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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