A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447769



Internal ID21105322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92378751..92394564hg38UCSC Ensembl
chr9:95141033..95156846hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3815814
hg1915814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196122
Samples
Known GenesCENPP, OGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447769
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