A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027368



Internal ID21936711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77762317..77762514hg38UCSC Ensembl
chr14:78228660..78228857hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602248
Samples
Known GenesC14orf178
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027368
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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