A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126231



Internal ID21452062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42166381..42166381hg38UCSC Ensembl
chr22:42562387..42562387hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665695
Supporting Variants
SamplesHG01596
Known GenesTCF20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126231
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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