A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037518



Internal ID19126737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20402228hg38UCSC Ensembl
Innerchr15:20532605..20607481hg19UCSC Ensembl
Innerchr15:18792619..18867495hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3874877
hg1974877
hg1874877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2241n100
Supporting Variantsnssv3536137
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)nsv1037518
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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