A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477999



Internal ID21135552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24314418..24315930hg38UCSC Ensembl
chr14:24783624..24785136hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016217
Samples
Known GenesLTB4R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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