A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046156



Internal ID19135375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20336715..20689298hg38UCSC Ensembl
Innerchr15:20541968..20894627hg19UCSC Ensembl
Innerchr15:18801982..19172949hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38352584
hg19352660
hg18370968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2233n100
Supporting Variantsnssv3713729
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)nsv1046156
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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