A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv791814



Internal ID16085770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31851236..31915943hg38UCSC Ensembl
Innerchr12:32004170..32068877hg19UCSC Ensembl
Innerchr12:31895437..31960144hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3864708
hg1964708
hg1864708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558148
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv791814
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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