A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131529



Internal ID21450895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28537293..28537293hg38UCSC Ensembl
chr22:28933281..28933281hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666815
Supporting Variants
SamplesHG01505
Known GenesTTC28
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131529
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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