A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082621



Internal ID21991854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36666083..36666083hg38UCSC Ensembl
chr14:37135288..37135288hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603380
Samples
Known GenesPAX9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082621
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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