A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441951



Internal ID22108133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26495548..26495684hg38UCSC Ensembl
chr22:26891514..26891650hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767715
Samples
Known GenesTFIP11
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441951
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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