A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529498



Internal ID22398890
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2722n152
Supporting Variantsnssv14377376, nssv14385796
SamplesHG00731, HG00733
Known GenesCHGA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529498
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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