A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435481



Internal ID21093034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12495272..12848783hg38UCSC Ensembl
chr9:12495272..12848782hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38353512
hg19353511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176636
Samples
Known GenesLURAP1L, TYRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435481
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