A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046913



Internal ID19136132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20404354hg38UCSC Ensembl
Innerchr15:20532605..20609607hg19UCSC Ensembl
Innerchr15:18792619..18869621hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3877003
hg1977003
hg1877003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2241n100
Supporting Variantsnssv3536139, nssv3536138
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)nsv1046913
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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