A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843713



Internal ID22618648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114164625..114212005hg38UCSC Ensembl
chr6:114485789..114533169hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3847381
hg1947381
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843713
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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