A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846068



Internal ID22621003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70935858..70946951hg38UCSC Ensembl
chr6:71645561..71656654hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811094
hg1911094
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507941, nssv17507942
Samples
Known GenesB3GAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846068
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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