A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036567



Internal ID19125786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:133090506..133150038hg38UCSC Ensembl
Innerchr12:133667092..133726624hg19UCSC Ensembl
Innerchr12:132177165..132236697hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3859533
hg1959533
hg1859533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1594n100
Supporting Variantsnssv3526398
Samples
Known GenesZNF10, ZNF140, ZNF891
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036567
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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