A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037278



Internal ID19126497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97692589..98009540hg38UCSC Ensembl
Innerchr11:97563589..97880268hg19UCSC Ensembl
Innerchr11:97068799..97385478hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38316952
hg19316680
hg18316680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504862
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)nsv1037278
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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