A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090178



Internal ID21999411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72008847..72008847hg38UCSC Ensembl
chr15:72301188..72301188hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601912
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090178
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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