A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650217



Internal ID21598522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133366702..133366702hg38UCSC Ensembl
chr10:135180206..135180206hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067997
SamplesHG00732
Known GenesECHS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650217
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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