A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603112



Internal ID21551774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91385878..91386199hg38UCSC Ensembl
chr9:94148160..94148481hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163393
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603112
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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