A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425466



Internal ID21083019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35360930..35364013hg38UCSC Ensembl
chr8:35218448..35221531hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383084
hg193084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166797
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425466
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