A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577920



Internal ID21769963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26002593..26002593hg38UCSC Ensembl
chr10:26291522..26291522hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097353
Supporting Variants
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577920
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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