A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838949



Internal ID22613884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33865676..33868211hg38UCSC Ensembl
chr4:33867298..33869833hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382536
hg192536
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838949
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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