A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3539907



Internal ID18838188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20060713..22294566hg38UCSC Ensembl
Innerchr15:20265966..22582517hg19UCSC Ensembl
Innerchr15:18525980..20083881hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382233854
hg192316552
hg181557902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037327
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nssv3539907
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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