A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379643



Internal ID22437513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59268720..59268720hg38UCSC Ensembl
chr15:59560919..59560919hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968443
Supporting Variants
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379643
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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