A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485996



Internal ID21143549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54134683..54141001hg38UCSC Ensembl
chr14:54601401..54607719hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg386319
hg196319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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