A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053541



Internal ID20620581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167079688..167085149hg38UCSC Ensembl
chr1:167048925..167054386hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg385462
hg195462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334522
Supporting Variants
Samples
Known GenesGPA33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053541
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