A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3535979



Internal ID18834260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376297..22270474hg38UCSC Ensembl
Innerchr15:20581550..22558425hg19UCSC Ensembl
Innerchr15:18841564..20059789hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381894178
hg191976876
hg181218226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041105
Supporting Variants
Samples
Known GenesCT60, 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)nssv3535979
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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