A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138666



Internal ID21451211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44920603..44920603hg38UCSC Ensembl
chr22:45316483..45316483hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665946
Supporting Variants
SamplesHG01505
Known GenesPHF21B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138666
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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