A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439311



Internal ID21096864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83796571..83823021hg38UCSC Ensembl
chr9:86411486..86437936hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3826451
hg1926451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193804
Samples
Known GenesGKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439311
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