A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557410



Internal ID16344819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9471020..9585474hg38UCSC Ensembl
Innerchr12:9623616..9738070hg19UCSC Ensembl
Innerchr12:9514883..9629337hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38114455
hg19114455
hg18114455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2349n54
Supporting Variantsnssv787613
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557410
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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