A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522061



Internal ID20895422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44737134..44837738hg38UCSC Ensembl
chr19:45240391..45340995hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38100605
hg19100605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198852
Samples
Known GenesBCAM, BCL3, CBLC, MIR8085
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522061
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