A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038400



Internal ID19127619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:80025250..80051324hg38UCSC Ensembl
Innerchr12:80419030..80445104hg19UCSC Ensembl
Innerchr12:78943161..78969235hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3826075
hg1926075
hg1826075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1529n100
Supporting Variantsnssv3524647
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)nsv1038400
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