A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043438



Internal ID21952742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235412182..235412182hg38UCSC Ensembl
chr1:235575497..235575497hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521666
Samples
Known GenesTBCE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043438
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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