A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107291



Internal ID22016524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50030456..50030456hg38UCSC Ensembl
chr18:47556826..47556826hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634332
Samples
Known GenesMYO5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107291
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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