A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040649



Internal ID19129868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126044947..126112810hg38UCSC Ensembl
Innerchr11:125914842..125982705hg19UCSC Ensembl
Innerchr11:125420052..125487915hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3867864
hg1967864
hg1867864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710764
Samples
Known GenesCDON
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040649
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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