A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527857



Internal ID20901218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28751668..28809727hg38UCSC Ensembl
chr19:29242575..29300634hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3858060
hg1958060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527857
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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