A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844993



Internal ID22619928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52757808..52811711hg38UCSC Ensembl
chr6:52622606..52676509hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3853904
hg1953904
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506473, nssv17506474
Samples
Known GenesGSTA1, GSTA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844993
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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