A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567746



Internal ID21516085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219456893..219456960hg38UCSC Ensembl
chr2:220321615..220321682hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111463
SamplesHG00732
Known GenesSPEG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567746
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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