A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037142



Internal ID19126361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31104761..31257350hg38UCSC Ensembl
Innerchr12:31257695..31410284hg19UCSC Ensembl
Innerchr12:31148962..31301551hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38152590
hg19152590
hg18152590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1417n100
Supporting Variantsnssv3710356, nssv3521958, nssv3710359, nssv3710358, nssv3511068, nssv3506330, nssv3504414, nssv3710355, nssv3710357, nssv3710360, nssv3710354
Samples
Known GenesDDX11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037142
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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