A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526832



Internal ID20900193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17282301..17283200hg38UCSC Ensembl
chr20:17262946..17263845hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066641
Samples
Known GenesPCSK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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