A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041862



Internal ID19131081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106340093..106367969hg38UCSC Ensembl
Innerchr11:106210820..106238696hg19UCSC Ensembl
Innerchr11:105716030..105743906hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3827877
hg1927877
hg1827877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508726
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)nsv1041862
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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