A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030604



Internal ID21939947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82791518..82804567hg38UCSC Ensembl
chr14:83257862..83270911hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3813050
hg1913050
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030604
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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