A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223026



Internal ID22366915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101711101..101719100hg38UCSC Ensembl
chr14:102177438..102185437hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14388380, nssv14389049, nssv14387820, nssv14377149, nssv14374306, nssv14387118, nssv14388727, nssv14390483, nssv14392239
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223026
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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