A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538346



Internal ID20911663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11915101..11941700hg38UCSC Ensembl
chr1:143150049..143184545hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3826600
hg1934497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538346
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