A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014273



Internal ID19103494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87251334..87661069hg38UCSC Ensembl
Innerchr2:87478457..87960588hg19UCSC Ensembl
Innerchr2:87331968..87741703hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38409736
hg19482132
hg18409736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3900n100
Supporting Variantsnssv3728777
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014273
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer