A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035584



Internal ID18778115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34464686..34565797hg38UCSC Ensembl
Innerchr15:34756887..34857998hg19UCSC Ensembl
Innerchr15:32544179..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38101112
hg19101112
hg18101112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2572n100
Supporting Variantsnssv3552130
Samples
Known GenesGOLGA8B, 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)nsv1035584
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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