A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043981



Internal ID19133200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..22218839hg38UCSC Ensembl
Innerchr15:20284054..22506790hg19UCSC Ensembl
Innerchr15:18544068..20008154hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382140039
hg192222737
hg181464087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3716012
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)nsv1043981
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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