A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037108



Internal ID19126327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20936842..22168141hg38UCSC Ensembl
Innerchr15:21142171..22456092hg19UCSC Ensembl
Innerchr15:19406830..19957456hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381231300
hg191313922
hg18550627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2332n100
Supporting Variantsnssv3541462, nssv3541461
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037108
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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