A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052155



Internal ID19141374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:113715812..113738972hg38UCSC Ensembl
Innerchr12:114153617..114176777hg19UCSC Ensembl
Innerchr12:112638000..112661160hg18UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3823161
hg1923161
hg1823161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524946
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)nsv1052155
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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