A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592614



Internal ID21541197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32694067..32694144hg38UCSC Ensembl
chr9:32694065..32694142hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161607
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592614
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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