A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486545



Internal ID21144098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39449901..39452500hg38UCSC Ensembl
chr14:39919105..39921704hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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