A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187021



Internal ID20754061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69240217..69240864hg38UCSC Ensembl
chr9:71855133..71855780hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442742
Supporting Variants
Samples
Known GenesTJP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187021
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