A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14302861



Internal ID22297490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12810511..12810583hg38UCSC Ensembl
chr4:49168719..49168791hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3541993
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14302861
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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