A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547997



Internal ID16335406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158755774..158757804hg38UCSC Ensembl
Innerchr1:158725564..158727594hg19UCSC Ensembl
Innerchr1:156992188..156994218hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382031
hg192031
hg182031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv592n54
Supporting Variantsnssv725025
Samples
Known GenesOR6K6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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