A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560296



Internal ID16347705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115087270..115105654hg38UCSC Ensembl
Innerchr12:115525075..115543459hg19UCSC Ensembl
Innerchr12:114009458..114027842hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3818385
hg1918385
hg1818385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175894
SamplesHGDP01063
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560296
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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