A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545593



Internal ID16333002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15192296..15224029hg38UCSC Ensembl
Innerchr1:15518792..15550525hg19UCSC Ensembl
Innerchr1:15391379..15423112hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3831734
hg1931734
hg1831734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173771
SamplesHGDP00863
Known GenesTMEM51
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545593
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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