A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523066



Internal ID18821347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37678279..38044017hg38UCSC Ensembl
Innerchr12:38072081..38437819hg19UCSC Ensembl
Innerchr12:36358348..36724086hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38365739
hg19365739
hg18365739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049294
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)nssv3523066
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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