A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655210



Internal ID21603515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100166005..100166005hg38UCSC Ensembl
chr14:100632342..100632342hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082893
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655210
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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