A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644872



Internal ID21836919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26495548..26495685hg38UCSC Ensembl
chr22:26891514..26891651hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053743
Supporting Variants
Samples
Known GenesTFIP11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644872
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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