A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844196



Internal ID22619131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166954710..166961355hg38UCSC Ensembl
chr6:167368198..167374843hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386646
hg196646
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502990
Samples
Known GenesRNASET2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844196
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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