A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837838



Internal ID22612773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11206923..11271945hg38UCSC Ensembl
chr4:11208547..11273569hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3865023
hg1965023
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837838
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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