A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332444



Internal ID20865616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95288401..95291200hg38UCSC Ensembl
chr1:95753957..95756756hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332444
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