A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582808



Internal ID21531324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:111845679..111845992hg38UCSC Ensembl
chr2:112603256..112603569hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107645
SamplesNA12329
Known GenesANAPC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582808
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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