A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046362



Internal ID19135581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:113629281..113681535hg38UCSC Ensembl
Innerchr12:114067086..114119340hg19UCSC Ensembl
Innerchr12:112551469..112603723hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3852255
hg1952255
hg1852255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524945
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)nsv1046362
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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