A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436842



Internal ID21094395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75022901..75031300hg38UCSC Ensembl
chr9:77637817..77646216hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230339
Samples
Known GenesC9orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436842
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