A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588760



Internal ID21537324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88625479..88625665hg38UCSC Ensembl
chr9:91240394..91240580hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163096
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588760
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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