A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529508



Internal ID22398900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90455192..90455270hg38UCSC Ensembl
chr14:90921536..90921614hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14376077, nssv14385085
SamplesHG00513, HG00514
Known GenesLINC00642
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529508
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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