A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838062



Internal ID22612997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151162216..151164690hg38UCSC Ensembl
chr4:152083368..152085842hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382475
hg192475
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490305
Samples
Known GenesSH3D19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838062
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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