A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035683



Internal ID19124902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:45001..98691hg38UCSC Ensembl
Innerchr12:150430..207857hg19UCSC Ensembl
Innerchr12:20691..78118hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3853691
hg1957428
hg1857428
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1325n100
Supporting Variantsnssv3513551, nssv3710804, nssv3513170, nssv3503240, nssv3510860, nssv3521510
Samples
Known GenesIQSEC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035683
Frequency
Sample Size11257
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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