A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054230



Internal ID19143449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20936842..22156430hg38UCSC Ensembl
Innerchr15:21142171..22444381hg19UCSC Ensembl
Innerchr15:19406830..19945745hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381219589
hg191302211
hg18538916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2332n100
Supporting Variantsnssv3541460
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)nsv1054230
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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