A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516829



Internal ID20890190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7795190..7799123hg38UCSC Ensembl
chr19:7860076..7864009hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383934
hg193934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer