A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839664



Internal ID22614599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51850775..51853421hg38UCSC Ensembl
chr4:52716941..52719587hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382647
hg192647
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495876, nssv17495875
Samples
Known GenesDCUN1D4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839664
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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