A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329976



Internal ID20863130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18468378..18473256hg38UCSC Ensembl
chr1:18794872..18799750hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384879
hg194879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329976
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