A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370967



Internal ID22261607
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527157
Supporting Variants
SamplesNA19238
Known GenesKIAA0391
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370967
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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