A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076478



Internal ID21985711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167330888..167330888hg38UCSC Ensembl
chr3:167048676..167048676hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554633
Samples
Known GenesZBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076478
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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