A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490668



Internal ID21148221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25167411..25183669hg38UCSC Ensembl
chr14:25636617..25652875hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3816259
hg1916259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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