A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046132



Internal ID18788663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30949950..30980130hg38UCSC Ensembl
Innerchr12:31102884..31133065hg19UCSC Ensembl
Innerchr12:30994151..31024332hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3830181
hg1930182
hg1830182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1414n100
Supporting Variantsnssv3516714, nssv3505769
Samples
Known GenesTSPAN11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046132
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer