A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047018



Internal ID19136237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380825..20614753hg38UCSC Ensembl
Innerchr15:20586078..20820055hg19UCSC Ensembl
Innerchr15:18846092..19080069hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38233929
hg19233978
hg18233978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2266n100
Supporting Variantsnssv3538664
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047018
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer