A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037194



Internal ID19126413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:83466146..83516851hg38UCSC Ensembl
Innerchr12:83859925..83910630hg19UCSC Ensembl
Innerchr12:82384056..82434761hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3850706
hg1950706
hg1850706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524744
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)nsv1037194
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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