A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527817



Internal ID20901178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4677289..4678683hg38UCSC Ensembl
chr19:4677301..4678695hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046831
Samples
Known GenesDPP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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