A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224356



Internal ID22367814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21438140..21438788hg38UCSC Ensembl
chr14:21906299..21906947hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372502, nssv14372503
SamplesNA19240, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224356
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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