A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533106



Internal ID20906467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18298403..18303177hg38UCSC Ensembl
chr19:18409213..18413987hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384775
hg194775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3456n223
Supporting Variantsnssv18045086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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