A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045831



Internal ID19135050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45397563..45558857hg38UCSC Ensembl
Innerchr11:45419113..45580407hg19UCSC Ensembl
Innerchr11:45375689..45536983hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38161295
hg19161295
hg18161295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515604
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)nsv1045831
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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