A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587633



Internal ID21536191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95004706..95004757hg38UCSC Ensembl
chr9:97766988..97767039hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163770
SamplesNA19238
Known GenesC9orf3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587633
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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