A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319216



Internal ID20852308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235348480..235365069hg38UCSC Ensembl
chr1:235511795..235528384hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3816590
hg1916590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319216
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