A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073737



Internal ID20640777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31542829..31560488hg38UCSC Ensembl
chr22:31938815..31956474hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3817660
hg1917660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542644
Supporting Variants
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer