A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492889



Internal ID21150442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30439613..30440027hg38UCSC Ensembl
chr14:30908819..30909233hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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