A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039514



Internal ID18782045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109348210..109377067hg38UCSC Ensembl
Innerchr12:109786015..109814872hg19UCSC Ensembl
Innerchr12:108270398..108299255hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3828858
hg1928858
hg1828858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1555n100
Supporting Variantsnssv3524900
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)nsv1039514
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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