A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597915



Internal ID21546536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92243063..92256625hg38UCSC Ensembl
chr12:92636839..92650401hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3813563
hg1913563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091728
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597915
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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