A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839662



Internal ID22614597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51818062..51881389hg38UCSC Ensembl
chr4:52684228..52747555hg19UCSC Ensembl
Cytoband4q11
Allele length
AssemblyAllele length
hg3863328
hg1963328
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495863, nssv17495864
Samples
Known GenesDCUN1D4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839662
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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