A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419483



Internal ID21077036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12698769..13182817hg38UCSC Ensembl
chr9:12698769..13182816hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38484049
hg19484048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176776
Samples
Known GenesLURAP1L, MPDZ, TYRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419483
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