A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933155



Internal ID21353225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23280710..23280710hg38UCSC Ensembl
chr14:23749919..23749919hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195056
SamplesHG002
Known GenesHOMEZ
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933155
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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