A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217992



Internal ID22363486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98356264..98356334hg38UCSC Ensembl
chr14:98822601..98822671hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383636
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217992
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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