A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169372



Internal ID21313855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92943508..92962521hg38UCSC Ensembl
Outerchr6:92935332..92966280hg38UCSC Ensembl
Innerchr6:93653226..93672239hg19UCSC Ensembl
Outerchr6:93645050..93675998hg19UCSC Ensembl
Innerchr6:93709947..93728960hg18UCSC Ensembl
Outerchr6:93701771..93732719hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3830949
hg1930949
hg1830949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252179
SamplesMLY_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169372
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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