A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122601



Internal ID21406312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27051912..27051912hg38UCSC Ensembl
chr22:27447874..27447874hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667290
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122601
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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