A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050636



Internal ID18793167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..22308242hg38UCSC Ensembl
Innerchr15:20564575..22681064hg19UCSC Ensembl
Innerchr15:18824589..20232428hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381948921
hg192116490
hg181407840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2179n100
Supporting Variantsnssv3537619, nssv3537617, nssv3537622, nssv3537624, nssv3537623, nssv3537618, nssv3537620, nssv3713793, nssv3537621
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050636
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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