A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048275



Internal ID19137494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92986515..93062046hg38UCSC Ensembl
Innerchr11:92719681..92795212hg19UCSC Ensembl
Innerchr11:92359329..92434860hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3875532
hg1975532
hg1875532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710708
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)nsv1048275
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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