A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595287



Internal ID21543891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92552055..92552106hg38UCSC Ensembl
chr9:95314337..95314388hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163248
SamplesHG00732
Known GenesCENPP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595287
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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