A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048459



Internal ID18790990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122486313..122526576hg38UCSC Ensembl
Innerchr11:122357021..122397284hg19UCSC Ensembl
Innerchr11:121862231..121902494hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3840264
hg1940264
hg1840264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710760
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)nsv1048459
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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