A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053119



Internal ID20620159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173383684..173384354hg38UCSC Ensembl
chr1:173352823..173353493hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327881
Supporting Variants
Samples
Known GenesLOC100506023
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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