A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045694



Internal ID19134913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11018847..11062454hg38UCSC Ensembl
Innerchr11:11040394..11084001hg19UCSC Ensembl
Innerchr11:10996970..11040577hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3843608
hg1943608
hg1843608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515472
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)nsv1045694
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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