A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525848



Internal ID20899209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47595567..47601236hg38UCSC Ensembl
chr19:48098824..48104493hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385670
hg195670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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