A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480554



Internal ID21138107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20411110..20412868hg38UCSC Ensembl
chr14:20879269..20881027hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381759
hg191759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016552
Samples
Known GenesTEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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