A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565988



Internal ID21514307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102003002..102003185hg38UCSC Ensembl
chr2:102619464..102619647hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107801
SamplesHG00732
Known GenesIL1R2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565988
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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