A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941461



Internal ID22716885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72103403..72103461hg38UCSC Ensembl
chr15:72395744..72395802hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389051
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941461
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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