A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439238



Internal ID21096791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138097201..138155700hg38UCSC Ensembl
chr9:140991653..141050152hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3858500
hg1958500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7963n223
Supporting Variantsnssv18222932
Samples
Known GenesCACNA1B, TUBBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer