A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330634



Internal ID20863792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89050551..89050857hg38UCSC Ensembl
chr1:89516234..89516540hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330634
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