A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037212



Internal ID19126431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20336715..22030511hg38UCSC Ensembl
Innerchr15:20541968..22318462hg19UCSC Ensembl
Innerchr15:18801982..19819826hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381693797
hg191776495
hg181017845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3713731, nssv3536259
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)nsv1037212
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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