A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141259



Internal ID20708299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149226079..149226403hg38UCSC Ensembl
chr6:149547215..149547539hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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