A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590600



Internal ID21539169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81615656..81615728hg38UCSC Ensembl
chr9:84230571..84230643hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162673
SamplesHG02587
Known GenesTLE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590600
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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