A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559720



Internal ID16000443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89709029..89709254hg38UCSC Ensembl
Innerchr12:90102806..90103031hg19UCSC Ensembl
Innerchr12:88626937..88627162hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38226
hg19226
hg18226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800061
Samples
Known GenesLINC00936
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559720
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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