A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549070



Internal ID15989793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:206857640..206867314hg38UCSC Ensembl
Innerchr1:207030985..207040659hg19UCSC Ensembl
Innerchr1:205097608..205107282hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg389675
hg199675
hg189675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv734985, nssv734984
Samples
Known GenesIL20
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549070
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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