A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423816



Internal ID21081369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140767891..140768260hg38UCSC Ensembl
chr8:141777990..141778359hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167273
Samples
Known GenesPTK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423816
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