A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554747



Internal ID20927838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42531101..42555600hg38UCSC Ensembl
chr22:42927107..42951606hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3824500
hg1924500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4723n223
Supporting Variantsnssv18207498
Samples
Known GenesSERHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554747
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