A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887562



Internal ID22662554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110243512..110248642hg38UCSC Ensembl
chr6:110564715..110569845hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385131
hg195131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429219
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887562
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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