A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544936



Internal ID15985659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1015128..1029058hg38UCSC Ensembl
Innerchr1:950508..964438hg19UCSC Ensembl
Innerchr1:940371..954301hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3813931
hg1913931
hg1813931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv17n54
Supporting Variantsnssv708454
Samples
Known GenesAGRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544936
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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