A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656114



Internal ID21604419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36794664..36794664hg38UCSC Ensembl
chr13:37368801..37368801hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099211
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656114
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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