A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186362



Internal ID20753403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69013801..69014400hg38UCSC Ensembl
chr9:71628717..71629316hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437002
Supporting Variants
Samples
Known GenesPRKACG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0856


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