A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044832



Internal ID19134051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20344625..20406244hg38UCSC Ensembl
Innerchr15:20549878..20611497hg19UCSC Ensembl
Innerchr15:18809892..18871511hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3861620
hg1961620
hg1861620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2251n100
Supporting Variantsnssv3713739
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044832
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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