A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3243867



Internal ID22375696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28905151..28910679hg38UCSC Ensembl
chr14:29374357..29379885hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385529
hg195529
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370093, nssv14370094, nssv14370090, nssv14370092, nssv14370091
SamplesHG00512, HG00731, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3243867
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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