A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129665



Internal ID21510988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35673756..35673756hg38UCSC Ensembl
chr22:36069803..36069803hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670767
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129665
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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