A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535165



Internal ID20908526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3787427..3811995hg38UCSC Ensembl
chr19:3787425..3811993hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3824569
hg1924569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198092
Samples
Known GenesMATK, ZFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535165
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