A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838715



Internal ID22613650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178010981..178016631hg38UCSC Ensembl
chr4:178932135..178937785hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg385651
hg195651
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838715
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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