A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039317



Internal ID19128536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381647..20609659hg38UCSC Ensembl
Innerchr15:20586900..20814965hg19UCSC Ensembl
Innerchr15:18846914..19074979hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38228013
hg19228066
hg18228066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2266n100
Supporting Variantsnssv3714764
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)nsv1039317
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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