A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844799



Internal ID22619734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163258863..163261909hg38UCSC Ensembl
chr6:163679895..163682941hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383047
hg193047
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502953
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844799
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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