A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536169



Internal ID18834450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20688370hg38UCSC Ensembl
Innerchr15:20532605..20893699hg19UCSC Ensembl
Innerchr15:18792619..19153713hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38361019
hg19361095
hg18361095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054038
Supporting Variants
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3536169
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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