A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514566



Internal ID18812847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28731593..28791193hg38UCSC Ensembl
Innerchr12:28884526..28944126hg19UCSC Ensembl
Innerchr12:28775793..28835393hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3859601
hg1959601
hg1859601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042920
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514566
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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