A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659726



Internal ID21608031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101443672..101443672hg38UCSC Ensembl
chr14:101910009..101910009hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085760
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659726
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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