A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069423



Internal ID21978656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116717410..116717410hg38UCSC Ensembl
chr3:116436257..116436257hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069423
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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