A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385796



Internal ID22238805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92929294..92929374hg38UCSC Ensembl
chr14:93395639..93395719hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529498
Supporting Variants
SamplesHG00733
Known GenesCHGA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385796
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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