A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039916



Internal ID19129135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..20773569hg38UCSC Ensembl
Innerchr15:20590015..20978898hg19UCSC Ensembl
Innerchr15:18850029..19238943hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38388808
hg19388884
hg18388915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2233n100
Supporting Variantsnssv3714773
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039916
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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