A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560052



Internal ID16347461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:104762037..104764197hg38UCSC Ensembl
Innerchr12:105155815..105157975hg19UCSC Ensembl
Innerchr12:103679945..103682105hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382161
hg192161
hg182161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv801808
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560052
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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