A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029397



Internal ID21938740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122902326..122902577hg38UCSC Ensembl
chr12:123386873..123387124hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029397
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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