A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053223



Internal ID19142442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..22122906hg38UCSC Ensembl
Innerchr15:20284054..22410857hg19UCSC Ensembl
Innerchr15:18544068..19912221hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382044106
hg192126804
hg181368154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3716007
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, 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)nsv1053223
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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