A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635456



Internal ID21583761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89436839..89436839hg38UCSC Ensembl
chr10:91196596..91196596hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071771
SamplesNA19650
Known GenesSLC16A12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635456
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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