A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125071



Internal ID21444770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44889982..44890031hg38UCSC Ensembl
chr22:45285862..45285911hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586482
Supporting Variants
SamplesHG00732
Known GenesPHF21B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125071
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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