A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390287



Internal ID22129018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103999643..103999770hg38UCSC Ensembl
chr14:104465980..104466107hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528252
Supporting Variants
SamplesHG00512
Known GenesTDRD9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390287
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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