A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839658



Internal ID22614593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:495909..535996hg38UCSC Ensembl
chr4:489698..529785hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3840088
hg1940088
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495298
Samples
Known GenesPIGG, ZNF721
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839658
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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