A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559705



Internal ID16000428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89702019..89713058hg38UCSC Ensembl
Innerchr12:90095796..90106835hg19UCSC Ensembl
Innerchr12:88619927..88630966hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3811040
hg1911040
hg1811040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800016
Samples
Known GenesLINC00936
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559705
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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