A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535284



Internal ID20908645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58324174..58340654hg38UCSC Ensembl
chr19:58835540..58852020hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3816481
hg1916481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049896
Samples
Known GenesMIR6806, ZSCAN22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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