A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031700



Internal ID21941043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32860480..32878368hg38UCSC Ensembl
chr14:33329686..33347574hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3817889
hg1917889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031700
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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