A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518325



Internal ID20891686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55330298..55336613hg38UCSC Ensembl
chr19:55841666..55847981hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386316
hg196316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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