A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660509



Internal ID21608814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52255708..52255708hg38UCSC Ensembl
chr15:52547905..52547905hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383587
hg193587
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086274
SamplesHG00731
Known GenesMYO5C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660509
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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