A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712694



Internal ID19010975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:133141843..133201059hg38UCSC Ensembl
Innerchr12:133718429..133777645hg19UCSC Ensembl
Innerchr12:132228502..132287718hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3859217
hg1959217
hg1859217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046905
Supporting Variants
Samples
Known GenesZNF10, ZNF268
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712694
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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