A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596266



Internal ID21544874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100397002..100397708hg38UCSC Ensembl
chr9:103159284..103159990hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145574
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596266
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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