A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633551



Internal ID21581856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137883231..137883231hg38UCSC Ensembl
chr5:137218920..137218920hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127198
SamplesNA19983
Known GenesMYOT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633551
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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