A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156454



Internal ID22086855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4170292..4174062hg38UCSC Ensembl
Outerchr6:4167285..4177293hg38UCSC Ensembl
Innerchr6:4170526..4174296hg19UCSC Ensembl
Outerchr6:4167519..4177527hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3810009
hg1910009
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018308
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156454
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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