A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844344



Internal ID22619279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12388356..12392937hg38UCSC Ensembl
chr6:12388588..12393169hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg384582
hg194582
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501544
Samples
Known GenesRNU6-48P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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