A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597701



Internal ID21546318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104489850..104489965hg38UCSC Ensembl
chr9:107252131..107252246hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155914
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597701
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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