A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv558966



Internal ID16346375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52873515..52874392hg38UCSC Ensembl
Innerchr12:53267299..53268176hg19UCSC Ensembl
Innerchr12:51553566..51554443hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38878
hg19878
hg18878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv796171
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv558966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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