A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918111



Internal ID22693332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170445307..170449874hg38UCSC Ensembl
chr6:170754395..170758962hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384568
hg194568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918111
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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