A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038804



Internal ID18781335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430589..34576796hg38UCSC Ensembl
Innerchr15:34722790..34868997hg19UCSC Ensembl
Innerchr15:32510082..32656289hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38146208
hg19146208
hg18146208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3549693
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038804
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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