A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560411



Internal ID22429207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51252272..51252272hg38UCSC Ensembl
chr14:51718990..51718990hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14371540, nssv14371541
SamplesHG00513, HG00514
Known GenesTMX1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560411
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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