A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584649



Internal ID21533192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107255996..107258566hg38UCSC Ensembl
chr9:110018277..110020847hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382571
hg192571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145781
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584649
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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