A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527926



Internal ID22397312
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2633n152
Supporting Variantsnssv14369566, nssv14369568, nssv14369567, nssv14369571, nssv14369565, nssv14369572, nssv14369569, nssv14369570
SamplesHG00512, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesLRRC9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527926
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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