A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888635



Internal ID22663643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111449995..111453560hg38UCSC Ensembl
chr6:111771198..111774763hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383566
hg193566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411382
Samples
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888635
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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