A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559665



Internal ID16347074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:85514618..85676914hg38UCSC Ensembl
Innerchr12:85908396..86070692hg19UCSC Ensembl
Innerchr12:84432527..84594823hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38162297
hg19162297
hg18162297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2766n54
Supporting Variantsnssv799960
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559665
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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