A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844343



Internal ID22619278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123582615..123587912hg38UCSC Ensembl
chr6:123903760..123909057hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385298
hg195298
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501128
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844343
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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