A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528581



Internal ID22397970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169987644..169988536hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8270n152
Supporting Variantsnssv14332554, nssv14332551, nssv14332550, nssv14332552, nssv14332553, nssv14332549
SamplesHG00512, NA19239, HG00731, HG00732, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528581
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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