A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544939



Internal ID15985662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1028484..1038387hg38UCSC Ensembl
Innerchr1:963864..973767hg19UCSC Ensembl
Innerchr1:953727..963630hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg389904
hg199904
hg189904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv18n54
Supporting Variantsnssv708459, nssv708458
Samples
Known GenesAGRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544939
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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