A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389051



Internal ID22446921
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 StatusS
Merged Variantsnsv5941461
Supporting Variants
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389051
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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