A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518068



Internal ID20891429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45893981..45896836hg38UCSC Ensembl
chr19:46397239..46400094hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382856
hg192856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046539
Samples
Known GenesMYPOP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518068
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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