A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093986



Internal ID21492195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108849551..108849889hg38UCSC Ensembl
chr13:109501899..109502237hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597251
Supporting Variants
SamplesNA19238
Known GenesMYO16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093986
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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