A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038566



Internal ID19127785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..22233250hg38UCSC Ensembl
Innerchr15:20262224..22521201hg19UCSC Ensembl
Innerchr15:18522238..20022565hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382176280
hg192258978
hg181500328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3715885
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, 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)nsv1038566
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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