A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527157



Internal ID22396542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35233086..35233672hg38UCSC Ensembl
chr14:35702292..35702878hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370967, nssv14370968
SamplesNA19238, NA19240
Known GenesKIAA0391
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527157
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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