A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026346



Internal ID21935689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71068635..71068839hg38UCSC Ensembl
chr14:71535352..71535556hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612586
Samples
Known GenesPCNX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026346
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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