A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050631



Internal ID19139850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20351177..22256018hg38UCSC Ensembl
Innerchr15:20556430..22543969hg19UCSC Ensembl
Innerchr15:18816444..20045333hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381904842
hg191987540
hg181228890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2192n100
Supporting Variantsnssv3536361
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)nsv1050631
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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