A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534827



Internal ID20908188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32828507..32907120hg38UCSC Ensembl
chr19:33319413..33398026hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3878614
hg1978614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047685
Samples
Known GenesCEP89, SLC7A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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