A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486769



Internal ID21144322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83923496..83924162hg38UCSC Ensembl
chr14:84389840..84390506hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486769
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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