A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078385



Internal ID21987618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138737963..138737963hg38UCSC Ensembl
chr3:138456805..138456805hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553174
Samples
Known GenesPIK3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078385
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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