A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207165



Internal ID22355597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108115051..108121250hg38UCSC Ensembl
chr6:108436255..108442454hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8054n152
Supporting Variantsnssv14330812, nssv14330814, nssv14330815, nssv14330810, nssv14330816, nssv14330813, nssv14330818, nssv14330817, nssv14330811
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207165
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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