A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041200



Internal ID18783731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30941428..30984205hg38UCSC Ensembl
Innerchr12:31094362..31137140hg19UCSC Ensembl
Innerchr12:30985629..31028407hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3842778
hg1942779
hg1842779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1413n100
Supporting Variantsnssv3510965
Samples
Known GenesTSPAN11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041200
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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