A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476469



Internal ID21134022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75974148..75974764hg38UCSC Ensembl
chr14:76440491..76441107hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021163
Samples
Known GenesTGFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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