A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628733



Internal ID21577038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87824129..87824129hg38UCSC Ensembl
chr10:89583886..89583886hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071746
SamplesNA19983
Known GenesCFL1P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628733
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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