A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009615



Internal ID18752146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87110834..87652179hg38UCSC Ensembl
Innerchr2:87337957..87951698hg19UCSC Ensembl
Innerchr2:87191468..87732813hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38541346
hg19613742
hg18541346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3888n100
Supporting Variantsnssv3582208, nssv3582209
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009615
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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