A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516384



Internal ID18814665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:34162014..34650099hg38UCSC Ensembl
Innerchr12:34314949..34803034hg19UCSC Ensembl
Innerchr12:34206216..34694301hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg38488086
hg19488086
hg18488086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045841
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)nssv3516384
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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