A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520780



Internal ID20894141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66716568..66726387hg38UCSC Ensembl
chr17:64712686..64722505hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg389820
hg199820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037355
Samples
Known GenesPRKCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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