A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156567



Internal ID22086968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104461140..104481736hg38UCSC Ensembl
Outerchr6:104449598..104495548hg38UCSC Ensembl
Innerchr6:104909015..104929611hg19UCSC Ensembl
Outerchr6:104897473..104943423hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3845951
hg1945951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022612, nssv4022614, nssv4022613
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156567
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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