A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042358



Internal ID19131577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..22139206hg38UCSC Ensembl
Innerchr15:20585976..22427157hg19UCSC Ensembl
Innerchr15:18845990..19928521hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381758484
hg191841182
hg181082532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3537368, nssv3537367
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, 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)nsv1042358
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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