A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037144



Internal ID19126363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:66809500..66931407hg38UCSC Ensembl
Innerchr12:67203280..67325187hg19UCSC Ensembl
Innerchr12:65489547..65611454hg18UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38121908
hg19121908
hg18121908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712546
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)nsv1037144
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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