A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328083



Internal ID20861228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229088205..229094782hg38UCSC Ensembl
chr1:229223952..229230529hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg386578
hg196578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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