A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14305643



Internal ID22274028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36461001..36461657hg38UCSC Ensembl
chr22:36857048..36857704hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214338
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14305643
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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