A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728201



Internal ID151867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26495553..26495677hg38UCSC Ensembl
chr22:26891519..26891643hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550696
Supporting Variants
Samples
Known GenesTFIP11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728201
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.374453


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