A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528252



Internal ID22397638
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377869, nssv14390287, nssv14384585, nssv14373546
SamplesHG00512, NA19238, NA19239, HG00514
Known GenesTDRD9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528252
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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