A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038223



Internal ID19127442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:114133855..114197011hg38UCSC Ensembl
Innerchr12:114571660..114634816hg19UCSC Ensembl
Innerchr12:113056043..113119199hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3863157
hg1963157
hg1863157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1558n100
Supporting Variantsnssv3524949
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)nsv1038223
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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