A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051707



Internal ID19140926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:41827681..41860571hg38UCSC Ensembl
Innerchr12:42221483..42254373hg19UCSC Ensembl
Innerchr12:40507750..40540640hg18UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3832891
hg1932891
hg1832891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1494n100
Supporting Variantsnssv3523509
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)nsv1051707
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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