A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036020



Internal ID19125239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22990352..23199681hg38UCSC Ensembl
Innerchr15:22673387..22882716hg19UCSC Ensembl
Innerchr15:20224751..20434157hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38209330
hg19209330
hg18209407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3538811
Samples
Known GenesGOLGA6L1, GOLGA8DP, MIR4509-1, MIR4509-2, MIR4509-3, TUBGCP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036020
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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