A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14369568



Internal ID22191934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59975086..59975151hg38UCSC Ensembl
chr14:60441804..60441869hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527926
Supporting Variants
SamplesHG00731
Known GenesLRRC9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14369568
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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