A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031358



Internal ID21940701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51278141..51282908hg38UCSC Ensembl
chr14:51744859..51749626hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg384768
hg194768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031358
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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