A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121165



Internal ID21420077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17038567..17039026hg38UCSC Ensembl
chr22:17519457..17519916hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592669
Supporting Variants
SamplesHG00731
Known GenesCECR7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121165
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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