A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888492



Internal ID22663498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19730503..19730567hg38UCSC Ensembl
chr6:19730734..19730798hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888492
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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