A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012902



Internal ID19102119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:189635482..189673312hg38UCSC Ensembl
Innerchr1:189604612..189642442hg19UCSC Ensembl
Innerchr1:187871235..187909065hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3837831
hg1937831
hg1837831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv493n100
Supporting Variantsnssv3704855
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)nsv1012902
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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