A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837754



Internal ID22612689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151630146..151659529hg38UCSC Ensembl
chr4:152551298..152580681hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3829384
hg1929384
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499688
Samples
Known GenesFAM160A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837754
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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