A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054985



Internal ID18797516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34376855..34750571hg38UCSC Ensembl
Innerchr15:34669056..35042772hg19UCSC Ensembl
Innerchr15:32456348..32830064hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38373717
hg19373717
hg18373717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2552n100
Supporting Variantsnssv3547878
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054985
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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