A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565899



Internal ID21514216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165625863..165626154hg38UCSC Ensembl
chr2:166482373..166482664hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109701
SamplesNA18939
Known GenesCSRNP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565899
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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