A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559660



Internal ID16347069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:85135571..85209753hg38UCSC Ensembl
Innerchr12:85529349..85603531hg19UCSC Ensembl
Innerchr12:84053480..84127662hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3874183
hg1974183
hg1874183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2765n54
Supporting Variantsnssv799955, nssv799956
Samples
Known GenesLRRIQ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559660
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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