A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051256



Internal ID20618296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119296699..119301313hg38UCSC Ensembl
chr1:119839322..119843936hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg384615
hg194615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320643
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051256
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