A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035483



Internal ID19124702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..20996195hg38UCSC Ensembl
Innerchr15:20586733..21201524hg19UCSC Ensembl
Innerchr15:18846747..19466183hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38614716
hg19614792
hg18619437
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2246n100
Supporting Variantsnssv3538718, nssv3714751
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)nsv1035483
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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