A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710368



Internal ID19008649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31125097..31241490hg38UCSC Ensembl
Innerchr12:31278031..31394424hg19UCSC Ensembl
Innerchr12:31169298..31285691hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38116394
hg19116394
hg18116394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042499
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710368
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