A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390835



Internal ID22254148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96597751..96599450hg38UCSC Ensembl
chr14:97064088..97065787hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213692
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390835
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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