A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843639



Internal ID22618574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106334920..106337445hg38UCSC Ensembl
chr6:106782795..106785320hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382526
hg192526
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500860, nssv17500861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843639
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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