A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610166



Internal ID21802213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72008453..72008515hg38UCSC Ensembl
chr15:72300794..72300856hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025902
Supporting Variants
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610166
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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