A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008782



Internal ID19098000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34450388..34511978hg38UCSC Ensembl
Innerchr2:34675455..34737045hg19UCSC Ensembl
Innerchr2:34528959..34590549hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3861591
hg1961591
hg1861591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3761n100
Supporting Variantsnssv3728061
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)nsv1008782
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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