A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524937



Internal ID18823218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111927424..112012015hg38UCSC Ensembl
Innerchr12:112365228..112449819hg19UCSC Ensembl
Innerchr12:110849611..110934202hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3884592
hg1984592
hg1884592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045310
Supporting Variants
Samples
Known GenesTMEM116
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524937
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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