A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559712



Internal ID16000435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89708524..89709513hg38UCSC Ensembl
Innerchr12:90102301..90103290hg19UCSC Ensembl
Innerchr12:88626432..88627421hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38990
hg19990
hg18990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2773n54
Supporting Variantsnssv800033, nssv800032, nssv800035, nssv800036, nssv800034, nssv800031
Samples
Known GenesLINC00936
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559712
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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