A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525564



Internal ID20898925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11748748..11766209hg38UCSC Ensembl
chr19:11859563..11877024hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3817462
hg1917462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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