A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013349



Internal ID19102567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89399710..89904396hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg18504687
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3968n100
Supporting Variantsnssv3582744, nssv3579745, nssv3582740, nssv3582745, nssv3582742, nssv3582743, nssv3579744, nssv3579743, nssv3582741
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)nsv1013349
Frequency
Sample Size11257
Observed Gain2
Observed Loss7
Observed Complex0
Frequencyn/a


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