A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046284



Internal ID19135503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20410584hg38UCSC Ensembl
Innerchr15:20585976..20615837hg19UCSC Ensembl
Innerchr15:18845990..18875851hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3829862
hg1929862
hg1829862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2274n100
Supporting Variantsnssv3536024
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046284
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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