A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073231



Internal ID20640271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27938932..27939407hg38UCSC Ensembl
chr22:28334920..28335395hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539261
Supporting Variants
Samples
Known GenesTTC28-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00017


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