A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038655



Internal ID18781186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..22300068hg38UCSC Ensembl
Innerchr15:20016316..22588019hg19UCSC Ensembl
Innerchr15:18276329..20089383hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382489006
hg192571704
hg181813055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2175n100
Supporting Variantsnssv3534430, nssv3534431, nssv3534432, nssv3715695
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038655
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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