A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039768



Internal ID18782299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..22129590hg38UCSC Ensembl
Innerchr15:20016316..22417541hg19UCSC Ensembl
Innerchr15:18276329..19918905hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382318528
hg192401226
hg181642577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2175n100
Supporting Variantsnssv3534429
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)nsv1039768
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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