A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839377



Internal ID22614312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58462738..58467794hg38UCSC Ensembl
chr4:59328904..59333960hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385057
hg195057
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839377
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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