A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041784



Internal ID19131003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:64985485..65027310hg38UCSC Ensembl
Innerchr12:65379265..65421090hg19UCSC Ensembl
Innerchr12:63665532..63707357hg18UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3841826
hg1941826
hg1841826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524988
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)nsv1041784
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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