A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425386



Internal ID21082939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30891236..30891646hg38UCSC Ensembl
chr9:30891234..30891644hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425386
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