A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041029



Internal ID19130248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:91890479..91914920hg38UCSC Ensembl
Innerchr12:92284255..92308696hg19UCSC Ensembl
Innerchr12:90808386..90832827hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3824442
hg1924442
hg1824442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524824
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)nsv1041029
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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