A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156478



Internal ID22086879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27664765..27689868hg38UCSC Ensembl
Outerchr6:27660614..27699777hg38UCSC Ensembl
Innerchr6:27632544..27657647hg19UCSC Ensembl
Outerchr6:27628393..27667556hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3839164
hg1939164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4019534, nssv4019533
Samples
Known GenesLINC01012
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156478
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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