A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14372485



Internal ID22277480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21183088..21183482hg38UCSC Ensembl
chr14:21651247..21651641hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228690
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14372485
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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