A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046518



Internal ID19135737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20406104..21078935hg38UCSC Ensembl
Innerchr15:20611357..21284264hg19UCSC Ensembl
Innerchr15:18871371..19548923hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38672832
hg19672908
hg18677553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2237n100
Supporting Variantsnssv3540848, nssv3540847
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, 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)nsv1046518
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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