A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042016



Internal ID19131235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..22129590hg38UCSC Ensembl
Innerchr15:20216943..22417541hg19UCSC Ensembl
Innerchr15:18476957..19918905hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382117901
hg192200599
hg181441949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3715782
Samples
Known GenesCHEK2P2, CT60, 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)nsv1042016
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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