A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846061



Internal ID22620996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69488475..69497447hg38UCSC Ensembl
chr6:70198367..70207339hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg388973
hg198973
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846061
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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