A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535280



Internal ID20908641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32957604..32958478hg38UCSC Ensembl
chr19:33448510..33449384hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047692
Samples
Known GenesCEP89
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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