A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559664



Internal ID16347073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:85514618..85630971hg38UCSC Ensembl
Innerchr12:85908396..86024749hg19UCSC Ensembl
Innerchr12:84432527..84548880hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38116354
hg19116354
hg18116354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2766n54
Supporting Variantsnssv799959, nssv1176327
Samples1780862414_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559664
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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