A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888463



Internal ID22663469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108344056..108357093hg38UCSC Ensembl
chr6:108665260..108678297hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3813038
hg1913038
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429298
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888463
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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