A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487452



Internal ID21145005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81474355..81474839hg38UCSC Ensembl
chr14:81940699..81941183hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021405
Samples
Known GenesSEL1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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