A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843647



Internal ID22618582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109343197..109344396hg38UCSC Ensembl
chr6:109664400..109665599hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500907, nssv17500908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843647
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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