A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14304885



Internal ID22224801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32585936..32585992hg38UCSC Ensembl
chr22:32981922..32981978hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226237
Supporting Variants
SamplesHG00733
Known GenesSYN3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14304885
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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