A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568547



Internal ID21516896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220081588..220081865hg38UCSC Ensembl
chr2:220946309..220946586hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111277
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568547
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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