A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559719



Internal ID16000442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89708976..89709148hg38UCSC Ensembl
Innerchr12:90102753..90102925hg19UCSC Ensembl
Innerchr12:88626884..88627056hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38173
hg19173
hg18173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800060
Samples
Known GenesLINC00936
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559719
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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