A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333481



Internal ID20866658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8271413..8275657hg38UCSC Ensembl
chr1:8331473..8335717hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg384245
hg194245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333481
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