A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493276



Internal ID21150829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20522419..20528398hg38UCSC Ensembl
chr14:20990578..20996557hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385980
hg195980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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