A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550738



Internal ID20923878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36117782..36122742hg38UCSC Ensembl
chr22:36513830..36518790hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg384961
hg194961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550738
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