A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156458



Internal ID22086859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10067773..10069647hg38UCSC Ensembl
Outerchr6:10063106..10072210hg38UCSC Ensembl
Innerchr6:10068006..10069880hg19UCSC Ensembl
Outerchr6:10063339..10072443hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg389105
hg199105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018313, nssv4018312
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156458
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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