A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596270



Internal ID21544878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35502476..35502525hg38UCSC Ensembl
chr22:35898523..35898572hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138272
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596270
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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