A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670429



Internal ID21618734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35463497..35463497hg38UCSC Ensembl
chr22:35859490..35859490hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124184
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670429
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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