A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067127



Internal ID20634167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24661785..24663867hg38UCSC Ensembl
chr20:24642421..24644503hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg382083
hg192083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534720
Supporting Variants
Samples
Known GenesSYNDIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067127
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