A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443799



Internal ID21101352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74951301..74954600hg38UCSC Ensembl
chr9:77566217..77569516hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184886
Samples
Known GenesC9orf40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443799
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