A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604308



Internal ID21552976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85858555..85861244hg38UCSC Ensembl
chr9:88473470..88476159hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382690
hg192690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162900
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604308
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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