A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576265



Internal ID21524702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21000846..21000995hg38UCSC Ensembl
chr2:21223718..21223867hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110011
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576265
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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