A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559715



Internal ID16000438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89708664..89709462hg38UCSC Ensembl
Innerchr12:90102441..90103239hg19UCSC Ensembl
Innerchr12:88626572..88627370hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38799
hg19799
hg18799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2775n54
Supporting Variantsnssv800045
Samples
Known GenesLINC00936
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer