A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639187



Internal ID21587492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26002660..26002660hg38UCSC Ensembl
chr10:26291589..26291589hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068194
SamplesNA19238
Known GenesMYO3A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639187
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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