A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527502



Internal ID22396888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132378505..132378618hg38UCSC Ensembl
chr9:135253892..135254005hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9767n152
Supporting Variantsnssv14349251, nssv14349252, nssv14349253, nssv14349250
SamplesHG00512, NA19238, NA19239, NA19240
Known GenesTTF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527502
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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