A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039316



Internal ID19128535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..20952464hg38UCSC Ensembl
Innerchr15:20590015..21157793hg19UCSC Ensembl
Innerchr15:18850029..19422452hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38567703
hg19567779
hg18572424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2237n100
Supporting Variantsnssv3539564
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)nsv1039316
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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