A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449500



Internal ID21107053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96645749..96649450hg38UCSC Ensembl
chr9:99408031..99411732hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383702
hg193702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193146
Samples
Known GenesAAED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449500
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