A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589631



Internal ID16377040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784337..8816277hg38UCSC Ensembl
Innerchr3:8826023..8857963hg19UCSC Ensembl
Innerchr3:8801023..8832963hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3831941
hg1931941
hg1831941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8214n54
Supporting Variantsnssv1151860, nssv958871, nssv1151861, nssv1151856, nssv1151858, nssv1151857, nssv958869, nssv958870, nssv1151859
Samples1780862521_A, 1780862275_A, NINDS_94, HGDP00072, 1780854118_A, NINDS_193
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589631
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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