A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052077



Internal ID19141296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20373039..22014043hg38UCSC Ensembl
Innerchr15:20578292..22301994hg19UCSC Ensembl
Innerchr15:18838306..19803358hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381641005
hg191723703
hg18965053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3535851
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nsv1052077
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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