A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057144



Internal ID21966377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156326731..156326731hg38UCSC Ensembl
chr1:156296522..156296522hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535284
Samples
Known GenesCCT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057144
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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