A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559659



Internal ID16347068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:85130362..85181250hg38UCSC Ensembl
Innerchr12:85524140..85575028hg19UCSC Ensembl
Innerchr12:84048271..84099159hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3850889
hg1950889
hg1850889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2764n54
Supporting Variantsnssv799954
Samples
Known GenesLRRIQ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559659
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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