A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970569



Internal ID22745504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72008845..72008845hg38UCSC Ensembl
chr15:72301186..72301186hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385711
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970569
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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