A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536190



Internal ID18834471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..22033266hg38UCSC Ensembl
Innerchr15:20532605..22321217hg19UCSC Ensembl
Innerchr15:18792619..19822581hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381705915
hg191788613
hg181029963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049128
Supporting Variants
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nssv3536190
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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