A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333901



Internal ID20867082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210273539..210297144hg38UCSC Ensembl
chr1:210446884..210470489hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3823606
hg1923606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333901
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