A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844259



Internal ID22619194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123585397..123587039hg38UCSC Ensembl
chr6:123906542..123908184hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381643
hg191643
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501129, nssv17501130
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844259
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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